WO2012072795A2 - Transformation of material into an optically modulating state via laser radiation - Google Patents

Transformation of material into an optically modulating state via laser radiation Download PDF

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Publication number
WO2012072795A2
WO2012072795A2 PCT/EP2011/071618 EP2011071618W WO2012072795A2 WO 2012072795 A2 WO2012072795 A2 WO 2012072795A2 EP 2011071618 W EP2011071618 W EP 2011071618W WO 2012072795 A2 WO2012072795 A2 WO 2012072795A2
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WO
WIPO (PCT)
Prior art keywords
optically modulating
plastic material
laser
channel
excitation
Prior art date
Application number
PCT/EP2011/071618
Other languages
English (en)
French (fr)
Other versions
WO2012072795A3 (en
Inventor
Torsten Schulz
Daniel Weicherding
Original Assignee
ALERE TECHNOLOGIES GmbH
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by ALERE TECHNOLOGIES GmbH filed Critical ALERE TECHNOLOGIES GmbH
Priority to US13/991,347 priority Critical patent/US9952153B2/en
Priority to EP11802005.6A priority patent/EP2646155A2/de
Priority to CN201180057678.8A priority patent/CN103442809B/zh
Publication of WO2012072795A2 publication Critical patent/WO2012072795A2/en
Publication of WO2012072795A3 publication Critical patent/WO2012072795A3/en

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Classifications

    • GPHYSICS
    • G01MEASURING; TESTING
    • G01NINVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N21/00Investigating or analysing materials by the use of optical means, i.e. using sub-millimetre waves, infrared, visible or ultraviolet light
    • G01N21/62Systems in which the material investigated is excited whereby it emits light or causes a change in wavelength of the incident light
    • G01N21/63Systems in which the material investigated is excited whereby it emits light or causes a change in wavelength of the incident light optically excited
    • G01N21/64Fluorescence; Phosphorescence
    • G01N21/6402Atomic fluorescence; Laser induced fluorescence
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01LCHEMICAL OR PHYSICAL LABORATORY APPARATUS FOR GENERAL USE
    • B01L3/00Containers or dishes for laboratory use, e.g. laboratory glassware; Droppers
    • B01L3/50Containers for the purpose of retaining a material to be analysed, e.g. test tubes
    • B01L3/502Containers for the purpose of retaining a material to be analysed, e.g. test tubes with fluid transport, e.g. in multi-compartment structures
    • B01L3/5027Containers for the purpose of retaining a material to be analysed, e.g. test tubes with fluid transport, e.g. in multi-compartment structures by integrated microfluidic structures, i.e. dimensions of channels and chambers are such that surface tension forces are important, e.g. lab-on-a-chip
    • B01L3/502707Containers for the purpose of retaining a material to be analysed, e.g. test tubes with fluid transport, e.g. in multi-compartment structures by integrated microfluidic structures, i.e. dimensions of channels and chambers are such that surface tension forces are important, e.g. lab-on-a-chip characterised by the manufacture of the container or its components
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B41PRINTING; LINING MACHINES; TYPEWRITERS; STAMPS
    • B41MPRINTING, DUPLICATING, MARKING, OR COPYING PROCESSES; COLOUR PRINTING
    • B41M5/00Duplicating or marking methods; Sheet materials for use therein
    • B41M5/24Ablative recording, e.g. by burning marks; Spark recording
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B41PRINTING; LINING MACHINES; TYPEWRITERS; STAMPS
    • B41MPRINTING, DUPLICATING, MARKING, OR COPYING PROCESSES; COLOUR PRINTING
    • B41M5/00Duplicating or marking methods; Sheet materials for use therein
    • B41M5/26Thermography ; Marking by high energetic means, e.g. laser otherwise than by burning, and characterised by the material used
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B41PRINTING; LINING MACHINES; TYPEWRITERS; STAMPS
    • B41MPRINTING, DUPLICATING, MARKING, OR COPYING PROCESSES; COLOUR PRINTING
    • B41M5/00Duplicating or marking methods; Sheet materials for use therein
    • B41M5/26Thermography ; Marking by high energetic means, e.g. laser otherwise than by burning, and characterised by the material used
    • B41M5/267Marking of plastic artifacts, e.g. with laser
    • GPHYSICS
    • G02OPTICS
    • G02CSPECTACLES; SUNGLASSES OR GOGGLES INSOFAR AS THEY HAVE THE SAME FEATURES AS SPECTACLES; CONTACT LENSES
    • G02C7/00Optical parts
    • G02C7/02Lenses; Lens systems ; Methods of designing lenses
    • G02C7/021Lenses; Lens systems ; Methods of designing lenses with pattern for identification or with cosmetic or therapeutic effects
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01LCHEMICAL OR PHYSICAL LABORATORY APPARATUS FOR GENERAL USE
    • B01L2300/00Additional constructional details
    • B01L2300/06Auxiliary integrated devices, integrated components
    • B01L2300/0627Sensor or part of a sensor is integrated
    • B01L2300/0654Lenses; Optical fibres
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01LCHEMICAL OR PHYSICAL LABORATORY APPARATUS FOR GENERAL USE
    • B01L2300/00Additional constructional details
    • B01L2300/16Surface properties and coatings
    • B01L2300/168Specific optical properties, e.g. reflective coatings

Definitions

  • the present invention relates to the transformation of material (e.g. plastic material) into an optically modulating state via laser radiation, as well as optically modulating elements and/or material obtained by the application of laser radiation onto or into the material and devices comprising optically modulating material and/or elements.
  • material e.g. plastic material
  • optically modulating elements and/or material obtained by the application of laser radiation onto or into the material and devices comprising optically modulating material and/or elements.
  • the labeling and marking of material and products is becoming of rising importance in many industrial fields.
  • the labels and marks are predominantly generated using conventional techniques such as printing, stamping, engraving or embossing. Marking via the application of laser radiation has been established as interesting alternative to these techniques since it is rapid, can be applied on non- planar surfaces and is in general durable and abrasion-resistant due to the inscription in the material, in particular plastic material, itself.
  • Laser marking methods have been described for different materials, in particular for plastics or polymeric materials.
  • the underlying effect is generally based on an interaction between the polymeric matrix of the material or a laser sensitive additive to said material with a laser beam, which generates a high degree of thermal energy at the laser target point .
  • the application of energy is assumed to result in pyro lysis, carbonization and/or ablation of material, leading to macroscopic modifications of the material, which are optically detectable for the human eye.
  • US Patent No. 6, 284, 184 discloses a method of laser marking a plastic substrate based on a layered polymeric substrate, which is ablated in order to reveal a differently colored layer underneath.
  • US Patent No. 4,822,973 discloses a system, in which the laser radiation passes through the surface of a first layer material and becomes absorbed in a second layer material leading to a laser conveyed marking therein.
  • the described methods are focused on the generation of generally visible labels or modifications on the treated material, which may however not be applicable in situations in which an optical reaction other than optical reflection is required.
  • the optically modulating state may be a state in which light is modulated with respect to one or more of its characteristics comprising wavelength, amplitude, direction and/or phase. For instance, in some embodiments light is emitted by the structures at a different wavelength than it is absorbed (e.g. similar to fluorescence or phosphorescence) and/or at a different direction so that modulation of the light other than pure or nearly pure reflection occur.
  • a use comprises the employment of laser radiation for the transformation of plastic material into an optically modulating state.
  • the optically modulating state can be a fluorescent or a scattering state or similar to a fluorescent state or comparable to a fluorescent state.
  • the plastic material to be employed in the use or method may be a thermoplastic material or an elastomeric material.
  • the plastic material to be employed in the use or method may further be an organic polymer selected from the group consisting o polyethylene, polypropylene, polystyrene, polycarbonate and polycycloolefin.
  • the laser radiation to be employed in the use or method may comprise the application of an amount of energy of about 0.1 nJouie/ ⁇ 2 to about 100 ⁇ / ⁇ 2 .
  • the laser radiation to be employed in the use or method may comprise a radiation of a wavelength of about 355 nm to about 1064 nm.
  • the optically modulating state of the plastic material may absorb light in a wavelength spectrum of about 380 nm to about 540 nm and/or a wavelength spectrum of about 635 nm to about 655 nm.
  • the optically modulating state of the plastic material may emit upon excitation light in a wavelength spectrum of about 550 nm to about 800 nm.
  • the optically modulating state of the plastic material may emit upon excitation light at peak wavelengths of 593 nm and/or 685 nm.
  • the transformation of the plastic material comprises the generation of optically modulating elements on the surface of said plastic material, selected from the group comprising geometrical forms, geometrical pattern, spots, dots, lines, circles, squares, characters, symbols, drawings, barcode and datamatrixcode, or any combination thereof.
  • the transformation of the plastic material comprises the generation of optically modulating elements.
  • said optically modulating elements are geometrical elements, and/or have a diameter of at least 5 ⁇ .
  • the plastic material to be employed in the use or method may be transparent.
  • the transformed plastic material may be water-resistant and/or indissoluble.
  • an optically modulating plastic material is produced by a method as described herein.
  • the produced plastic material may comprise a datamatrix of optically modulating spot elements.
  • the produced plastic material may additionally or alternatively comprise optically modulating reference marks for the alignment of arrays or array components.
  • a method for marking the surface o a material comprises applying laser radiation to the material, wherein said marked surface is optically modulating.
  • the laser radiation to be employed in the method comprises the application of an amount of energy of about 0.1 nJoule/ ⁇ 2 to about 100 ⁇ / ⁇ 2 .
  • the optical excitation of the marked surface may be broadband light excitation.
  • the broadband light excitation of the marked surface may be an excitation in a wavelength spectrum of about 380 nm to about 540 nm and/or a wavelength spectrum of about 635 nm to about 655 nm.
  • the marked surface may emit upon excitation light in a wavelength spectrum of about 550 nm to about 800 nm.
  • the marked surface may emit upon excitation light at peak wavelengths of 593 nm and/or 685 nm.
  • a material is produced by a method for marking the surface of a material.
  • the material may be a plastic material.
  • the plastic material may be a thermoplastic material or an elastomeric material.
  • the plastic material may be an organic polymer selected from the group consisting of polyethylene, polypropylene, polystyrene, polycarbonate and polycycloolefin.
  • a material comprises a surface comprising one or more laser marks, wherein said laser mark is optically modulating.
  • the laser mark may be obtained from the application of laser radiation of an energy of about 0.1 nJoule/ ⁇ to about 100 ⁇ / ⁇ .
  • the laser mark may emit upon excitation light in a wavelength spectrum of about 550 nm to about 800 nm.
  • the laser mark may emit upon excitation light at peak wavelengths of 593 nm and/or 685 nm.
  • the excitation may be a broadband light excitation.
  • the broadband light excitation may be an excitation in a wavelength spectrum o about 380 nm to about 540 nm and/or a wavelength spectrum of about 635 nm to about 655 nm.
  • the material may be a plastic material.
  • the plastic material may be a thermoplastic material or an elastomeric material.
  • the plastic material may be an organic polymer selected from the group consisting of polyethylene, polypropylene, polystyrene, polycarbonate and polycycloolefin.
  • a datamatrix is composed of or comprises a laser mark on a material, wherein said laser mark is optically modulating.
  • the laser mark may emit upon excitation light in a wavelength spectrum of about 550 nm to about 800 nm.
  • the laser mark may emit upon excitation light at peak wavelengths of 593 nm and/or 685 nm.
  • the excitation may be a broadband light excitation.
  • the broadband light excitation may be an excitation in a wavelength spectrum of about 380 nm to about 540 nm and/or a wavelength spectrum of about 635 nm to about 655 nm.
  • the datamatrix may comprise a geometrical form, geometrical pattern, spot, dot, line, circle, square, character, symbol, drawing or barcode or any combination thereof.
  • a reference mark is composed of or comprises a laser mark on a material, wherein said laser mark is optically modulating.
  • the excitation may be a broadband light excitation.
  • the broadband light excitation may be an excitation in a wavelength spectrum of about 380 nm to about 540 nm and/or a wavelength spectrum of about 635 nm to about 655 nm.
  • the laser mark of the reference mark may be or may comprises a geometrical form, geometrical pattern, spot, dot, line, circle, square, character, symbol, drawing, or barcode or any combination thereof.
  • the reference mark may be an alignment mark.
  • the alignment mark may be an array alignment mark.
  • material as described herein is used as component for the manufacture of a device or instrument.
  • a method for the manufacture of a device or components thereof comprises the step of transforming material or a part of the material of said device into an optically modulating state by the application of laser radiation to said material.
  • the material may be plastic material.
  • the device to be produced may comprises a first channel having an inlet opening, and a longitudinal section in fluid communication with the inlet opening.
  • the device to be produced may comprises a first channel having an inlet opening, an outlet, and a longitudinal section between said inlet opening and said outlet, a channel including a capillary inlet; and a detection region in fluid communication with the capillary inlet.
  • the device to be produce may be a device for qualitatively and/or quantitatively detecting molecular interactions between probe molecules and target molecules, comprising:
  • micro-array comprising probe molecules immobilized in array elements, said micro-array being disposed on a first surface of the device;
  • reaction chamber formed between the first surface including the micro- array disposed thereon, and a second surface.
  • the device to be produced may comprise first and second substrates defining a channel therebetween, at least one of the substrates being flexible, the channel comprising an array of spaced-apart test zones, each test zone comprising a probe compound configured to participate in an assay for a target analyte.
  • the device to be produced may comprise a reaction chamber formed within a chamber body between a first surface and a second surface.
  • the device to be produced may comprise a reaction chamber formed within a chamber body between a first surface and a second surface, wherein the second surface is located opposite to the first surface,
  • the distance between the first surface and the second surface is variable at least in one or more parts of the surface area of the first surface and/or the second surface.
  • the device to be produced may comprise:
  • a cartridge having a micro flu idic channel including a capillary inlet; and a detection region in fluid communication with the capillary inlet;
  • microfluidic flow path having an at least partially deformable wall and in fluid communication with the detection region of the channel
  • the material as described herein is used for controlling optical parameters.
  • the optical parameter may be the focus of an optical device.
  • a microfluidic device comprises:
  • a first channel having an inlet opening, and a longitudinal section in fluid communication with the inlet opening wherein said device is at least partially composed of or comprises plastic material transformed into an optically modulating state.
  • a microfluidic device comprises:
  • a device for qualitatively and/or quantitatively detecting molecular interactions between probe molecules and target molecules comprises: a micro-array comprising probe molecules immobilized in array elements, said micro-array being disposed on a first surface o the device; and
  • reaction chamber formed between the first surface including the micro- array disposed thereon, and a second surface
  • said devic is at least partially composed of or comprises plastic material transformed into an optically modulating state.
  • the distance between said micro-array and the second surface may be variable.
  • a cartridge has a micro fluidic channel including a capillary inlet and a detection region in fluid communication with the capillary inlet, wherein said cartridge is at least partially composed o or comprises plastic material transformed into an optically modulating state.
  • a device comprises:
  • first and second substrates defining a channel therebetween, at least one of the substrates being flexible, the channel comprising an array of spaced-apart test zones, each test zone comprising a probe compound configured to participate in an assay for a target analyte,
  • said device is at least partially composed of or comprises plastic material which comprises one or more optically modulating elements.
  • a device for the qualitative and/or quantitative detection of particles comprises:
  • reaction chamber formed within a chamber body between a first surface and a second surface, wherein said device is at least partially composed of or comprises plastic material transformed into an optically modulating state.
  • a device for the qualitative and/or quantitative detection of particles comprises:
  • reaction chamber formed within a chamber body between a first surface and a second surface, wherein the second surface is located opposite to the first surface, and a microfluidic flow path having an at least partially deformable wall, being in fluid communication with the reaction chamber,
  • said device is at least partially composed of or comprises plastic material transformed into an optically modulating state.
  • the device may comprise one or more optically modulating elements located on either the first or the second surface of the reaction chamber.
  • a device for detecting an analyte comprises a cartridge having:
  • microfluidic channel including an inlet and a detection region in fluid communication with the inlet;
  • microfluidic flow path having an at least partially deformable wall and in fluid communication with the detection region of the channel
  • a cap comprising: a sealing member configured to seal with the inlet and form a fluid circuit including the inlet, the microfluidic channel and the microfluidic flow path and wherein said device is at least partially composed of or comprises plastic material transformed into an optically modulating state.
  • a system for detecting an analyte comprising a cartridge has:
  • microfluidic channel including an inlet and a detection region in fluid communication with the inlet;
  • microfluidic flow path having an at least partially deformable wall and in fluid communication with the detection region of the channel
  • a cap comprising:
  • a sealing member configured to seal with the inlet and form a fluid circuit including the inlet, the microfluidic channel and the microfluidic flow path;
  • a fluorescence detector including:
  • an objective lens wherein said system is at least partially composed of or comprises plastic material transformed into an optically modulating state.
  • a device for detecting an analyte in a sample comprises: a cartridge having:
  • a microfluidic channel including a capillary inlet; and a detection region in fluid communication with the capillary inlet;
  • microfluidic flow path having an at least partially deformable wall and in fluid communication with the detection region of the channel
  • control element wherein said control element is at least partially composed of or comprises plastic material transformed into an optically modulating state.
  • the material of the device or of the cartridge or of the system may comprise one or more optically modulating elements.
  • the material of the device or of the cartridge or of the system may comprise an array of optically modulating spots.
  • the material o f the device or of the cartridge or of the system may comprise a datamatrix or a reference mark.
  • T e material of the device or of the cartridge or of the system may comprise a datamatrix as described herein.
  • the material o the device or of the cartridge or of the system may comprise a reference mark as described herein.
  • the material of the device or of the cartridge or of the system may at least partially be composed of or comprises material as described herein.
  • a method for the qualitative and/or quantitative detection of particles comprises:
  • a method comprises labeling particles immobilized in the microfluidic channel of a device or system with an optical label or labeling reagent; obtaining a first image comprising at least a subset of the immobilized particles;
  • control elements for focusing and/or aligning said images, wherein said control element is at least partially composed of or comprises plastic material transformed into an optically modulating state.
  • a method comprises:
  • determining the number and/or size of the optically modulating elements comprised in said image determining a value indicative for the usability of the device or system and/or of any procedure, function or method carried out with or in said device or system and/or the accuracy of a test result obtained by using said device or system, based on a comparison of the determined number and/or size of the optically modulating elements, with said predetermined number and/or size.
  • the method may additionally comprise:
  • the method may further comprise displacing at least a part of the sample within the reaction chamber via one or more displacers.
  • the material may comprise an array of optically modulating spots.
  • the device or system may at least partially be composed of or comprise material as described herein.
  • the particle to be detected or immobilized in a device or method may be a prokaryotic cell, a eukaryotic cell, or a viral particle.
  • the particle to be detected or immobilized in a device or method may be a CD4' T-ce!l.
  • FIG. 1 illustrates the marking of a material by laser radiation.
  • FIG. 2 shows spots generated with a Nd:YAG laser of 8W power, at a wavelength of 1064 nm, a power of the diodes of 33%, a frequency of pulse of 35 kHz and a pulse width of 5 ⁇ $ on polystyrene plastic containing 5% carbon black.
  • FIG 2A depicts spots with a pitch of 40-45 ⁇ illuminated with the visible light spectrum. The image was taken with a standard microscope at 2x magnification.
  • FIG 2B depicts the same spots illuminated with light of a wavelength of 520 nm. The image was taken with PIMA analyzer.
  • FIG. 3 shows spots generated with a Nd:YAG laser of 8W power, at a wavelength of 1064 nm, a power of the diodes of 29%, a frequency of pulse of
  • FIG 3A depicts spots with a diameter of 25-30 ⁇ illuminated with the visible light spectrum. The image was taken with a standard microscope at 2x magnification.
  • FIG 3B depicts the same spots illuminated with light of a wavelength of 520 nm. The image was taken with PIMA analyzer.
  • FIG. 4 shows REM images of spots generated by laser radiation emitted from a 355nm laser at a frequency of 15kHz on polystyrene plastic containing 5% carbon black.
  • FIG 4A depicts the spots at a 100X magnification.
  • FIG. 413, FIG. 4C, FIG. 4D and FIG. 4E show different spot morphologies. The spot morphology is dependent on the energy input.
  • FIG. 5 depicts a correlation between signal intensity and laser power.
  • the intensity of the spots is reflected by the exposure time in the plastic material, correlated with the power of the laser.
  • the green signal corresponds to a wavelength of 593 nm
  • the red signal was measured at a wavelength of 685 nm.
  • the excitation was done by diode with a peak at 520 nm.
  • FIG. 6 shows a data matrix code generated by laser radiation emitted from a 355 nm laser at a frequency of 15 kHz on polystyrene plastic containing 5% carbon black.
  • the grid of the dots is 50 ⁇ .
  • the figure depicts the data matrix code illuminated with light of a wavelength of 520 nm. The image was taken by a PIMA analyzer.
  • FIG. 7 illustrates a microf!uidic cartdridge (100) suitable for determining the number of T helper cells in blood, comprising a detection channel (1 10) and a control for a capillary inlet (120).
  • the figure further shows a section of the detection channel (130), with an array of optically modulating laser spots (140) in an enlarged view.
  • FIG. 8 shows a shifted regular pattern of structures in an optically modulating state on the surface o f a channel of a micro iluidic device as depicted in Fig. 7.
  • the body of the device made from polystyrene plastic part containing 4% carbon black was treated with a 355 ran Nd : YAG laser.
  • FIG. 8 A and B show the surface of the channel comprising the structures in an optically modulating state imaged by a PIMA Analyzer.
  • the image was detected at a wavelength of 593nm and an exposure time of 300ms and a master gain of 2.74
  • the image shown in Fig. 8B was detected at 685nm with a exposure time of 300 ms and a master gain factor of 1 1.68.
  • a method for the transformation of plastic material into an optically modulating state comprises the application of laser radiation to plastic material.
  • the "transformation" can be a modification of the surface of the material, e.g. plastic material and/or a modification of one or more layers underneath the surface of the material, e.g. in cases in which layers of different transmissibility are present in the material.
  • the transformation may be a locally limited strong increase in temperature leading to structural and/or chemical modifications of the material, e.g. plastic material, for instance pyrolysis of the material, carbonization of the material, generation of aromatic structures in the material, generation of ablated regions, generation of craters, scratches, holes, embossments or rims.
  • the modification may take place in specific, predetermined regions or layers of the material, e.g. plastic material, due to the presence of additives, e.g.
  • the transformation may have a superficial or essentially planar or essentially two dimensional effect.
  • the transformation may have a spatial or essentially three dimensional effect.
  • An example of a spatial or essentially three dimensional effect is the modification of material into relief forms, or the modification of transparent material into a holographic, three dimensional form.
  • the material to be transformed can be any suitable material. Suitable material is any material which can be modified structurally and/or chemically, e.g. via pyrolysis, carbonization, generation of aromatic structures, generation of craters, scratches, holes, embossments or rims.
  • the material is plastic material.
  • Plastic material can be a natural, synthetic or semi-synthetic organic solid, e.g. a polymer of high molecular mass, which may or may not contain other substances to improve performance.
  • the plastic material can be soft, thermoset, elastomeric, biodegradable, electrically conductive, impervious to water or have further or other properties.
  • the transformation method leads to an optically modulating state of the treated material, e.g. plastic material.
  • An “optically modulating state” as used herein can be a state in which the wavelength of the light is changed and/or in which the direction of light radiation or reflection is changed.
  • light may be emitted by the modified point or region of the material, e.g. plastic material, at a different wavelength than it is absorbed.
  • the emitted light may have a longer wavelength, and therefore lower energy, than the absorbed radiation.
  • the wavelength of the absorbed light, the wavelength of the emitted light and/or the duration of the light emission after the absorption may vary.
  • the optically modulating state may be similar to or comparable to a fluorescent state in which the emitted light has a longer wavelength, than the absorbed radiation and wherein the light emission stops shortly after the light absorption stops.
  • the treated material in an optically modulating state is excited with a light of a wavelength in a range of about 350 to 750 nm, it may emit light of a longer wavelength, respectively, in a range of about 360 to 850 nm.
  • the optically modulating state may be similar to or comparable to a phosphorescent state in which the emitted light has a longer wavelength, than the absorbed radiation and wherein the light emission continues after the light absorption has stopped.
  • the optically modulating state may in certain, specific situations also be similar to or at least partially comprise a state in which modifications of the light other than pure or nearly pure reflection occurs, e.g. states in which incoming or impinging light is scattered.
  • the optically modulating state may further be a fluorescent state.
  • the laser radiation to be applied for the method can be any suitable laser radiation, e.g. ranging from wavelengths of 157 nm to 1064 nm. In some
  • the laser radiation is strong enough to cause evaporation, vaporization or melting of the impinged material.
  • the laser radiation is obtained from commercially available lasers. Examples include YAG lasers.
  • the specific type of laser may be a function of the material to be processed, of the envisaged temperature, of the envisaged modification type etc. Suitable laser forms, methods and apparatuses are known to the person skilled in the art.
  • the laser radiation to be applied is derived from a solid state neodymium : yttrium aluminium garnet (Nd:YAG) laser.
  • the laser radiation to be applied is derived from a solid state neodymium : yttrium vanadide (Nd:YV0 4 ) laser.
  • the power rating of the laser apparatuses may in some
  • embodiments vary between about 1 W and 6 ⁇ V, e.g. be at 0.5, 1 , 2 W, 3W, 4 W, 5W or 6 W.
  • the power may be adjusted via laser diodes.
  • the laser diodes may be set to transmission of between about 1 % to about 99%, e.g. to about 10%, 15%, 20%, 25%, 26%, 27%, 28%, 29%, 30%, 31%, 32%, 33%, 34%, 35%, 40%, 45%, 50%, 55%, 60%, 70%, 80%, 90% or more.
  • the application of the laser radiation may be performed continuously or periodically, e.g. in the form of pulses.
  • the application form and/or time may be set with regard to the degree of modification, the material to be treated, the laser model, the used wavelength and further suitable parameters known to the person skilled in the art.
  • Examples of application times are ranges of about 0.05 ⁇ 8 to 1 sec, 0.1 ⁇ to 0.5 sec, ⁇ ⁇ to 0.1 sec, 2 ⁇ 8, 3 ⁇ , 4 ⁇ , 5 ⁇ , 6 ⁇ , 7 ⁇ , 8 ⁇ , 9 ⁇ , 10 ⁇ , 20 ⁇ , 30 ⁇ , 50 ⁇ , 100 ⁇ , 200 ⁇ , 300 ⁇ , 400 ⁇ , 500 ⁇ , 600 ⁇ , 700 ⁇ , 800 ⁇ 8, 900 ⁇ , 1 ms, 10 ms, 100 ms.
  • the application times may he given in the form of laser radiation pulses. The pulses may be repeated once, twice, 3 times, 4 times, 5 times, 6 times, 7 times, 8 times, 10 times or more often.
  • the pulses may be followed by pauses or interims of different time periods, e.g. about ⁇ ⁇ to 10 sec, 2 ⁇ 8, 3 8, 4 ⁇ , 5 ⁇ , 6 ⁇ , 7 ⁇ , 8 ⁇ 1 ⁇ 4 9 ⁇ , 10 ⁇ , 20 ⁇ , 30 ⁇ , 50 ⁇ , 100 ⁇ , 200 ⁇ , 300 ⁇ , 400 ⁇ , 500 ⁇ , 600 ⁇ , 700 ⁇ », 800 ⁇ , 900 ⁇ , ⁇ ms, 10 ms, 100 ms, 1 sec or longer.
  • the pulse frequency may be set at about 1 kHz to about 150 kHz, e.g. at about 10 kHz, 15 kHz, 20 kHz, 25 kHz, 30 kHz, 35 kHz, 40 kHz, 45 kHz, 50 kHz, 55 kHz, 60 kHz, 70 kHz, 80kHz, 100 kHz, 120 kHz, 150 kHz.
  • the application of the laser radiation may, in another embodiment, be an application onto the material and/or into the material.
  • the method for the transformation of material, e.g. plastic material, into an optically modulating state may be carried out at a fixed distance between the laser radiation source and the material to be transformed, or at varying distances. The distance may be determined in respect of the type of laser source, the energy to be applied, the form of the envisaged modification etc.
  • the material to be transformed may be in a fixed position and the laser radiation source may be in a fixed position.
  • the material to be transformed may be moved in parallel to the laser radiation source or perpendicularly or axial ly thereto and the laser radiation source may be in a fixed position.
  • the material to be transformed may be in a fixed position and the laser radiation source may be moved in parallel to the material or perpendicularly or axially thereto.
  • the outcome of the application of laser radiation may be controlled, e.g. by microscopic inspection, fluorescence microscopic inspection or other suitable inspection techniques known to the person skilled in the art.
  • laser radiation may be applied a second or further time at the same point or region, or any portion thereof.
  • an advantageous method which allows the modification of material into an optically modulating state, i.e. into a state in which the impinging light is modified in at least one of its properties such as the wavelength of the emitted light or the direction of the reflected light.
  • the mentioned properties may be obtained and/or adjusted and/or modified via applying laser radiation as indicated above.
  • This method can advantageously be used fo a great variety of different applications.
  • Material may be marked superficially or internally, i.e. in deeper layers without modification of the outermost layer; material may externally or internally be decorated or covered with optically modulating points, symbols, codes, regions etc. whose visibility may depend on the impinging light, e.g. the wavelength of the impinging light; material may be decorated or covered with optically modulating points, symbols, codes, regions etc. which replace previously used optical control elements, e.g. attached entities.
  • a use of laser radiation for the transformation of material, e.g. plastic material, into an optically modulating state may comprise the employment of laser radiation as described herein for modifications of material, e.g. plastic material, as described herein in order to obtain material in an optically modulating state as described herein.
  • the plastic material to be employed in the use or method as described herein may be a thermoplastic material or an elastomeric material.
  • thermoplastic refers to a thermosoftening plastic polymer, which becomes liquid when heated and freezes to a glassy state when cooled sufficiently.
  • the thermoplastic may be a high-molecular- weight polymer whose chains associate through weak Van der Waals forces, stronger dipole-dipole interactions and hydrogen bonding; or stacking of aromatic rings.
  • the thermoplastic material may comprise additional components, e.g. iasersensitive compounds.
  • thermoplastics include Acryionitrile butadiene styrene (ABS) Acrylic (PMMA), Celluloid, Cellulose acetate, Cyclo olefin Copolymer (COC), Ethylene- Vinyl Acetate (EVA), Ethylene vinyl alcohol (EVOll), Fluoroplastics (PTFE, with FEP, PFA, CTFE, ECTFE, ETFE), lonomers, acr lic/PVC alloy, Liquid Crystal Polymer (LCP), Polyacetal (POM or Acetal), Polyacrylates (Acrylic),
  • PAN Polyacrylonitrile
  • PA Polyamide
  • PAI Polyamide-imide
  • PAE Polyaryletherketone
  • PBD Polybutadiene
  • PB Polybutylene
  • PBT Polybutylene terephthalate
  • PCL Polycaprolactone
  • PCTFE Polychlorotrifluoroethyiene
  • PET Polyethylene terephthalate
  • PCT Polycyclohexylene dimethylene terephthalate
  • PC Polycarbonate
  • PHAs Polyhydroxyalkanoates
  • PK Polyketone
  • PEEK Polyetheretherketone
  • PEKK Polyetherketoneketone
  • PEC Polyethylenechlorinates
  • PEC Polyimide
  • PAA Polylactic acid
  • PMP Polymethylpentene
  • PPO Polyphenylene oxide
  • PPS Polyphenylene sulfide
  • PPA Polyphthalamide
  • PP Polypropylene
  • PS Polystyrene
  • PSU Polysulfone
  • PTT Polytrimethylene terephthalate
  • PU Polyurethane
  • PVA Polyvinyl acetate
  • PVC Polyvinyl chloride
  • PVDC Polyvinylidene chloride
  • SAN Styrene-acrylonitrile
  • Elastomeric material refers to a polymer with the property of viscoelasticity, wherein the monomers, which link to form the polymer are typically made of carbon, hydrogen, oxygen and/or silicon. Elastomeric materials may be amorphous polymers existing above their glass transition temperature, so that considerable segmental motion is possible. At ambient temperatures they may be relatively soft and deformable.
  • elastomeric material examples include Natural rubber (NR.), Synthetic polyisoprene (IR), Butyl rubber (copolymer of isobutylene and isoprene, IIR), Polybutadiene (BR), Styrene-butadiene Rubber (copolymer of polystyrene and polybutadiene, SBR), Nitrile rubber (copolymer of polybutadiene and acryionitrile, BR), Hydrogenated Nitrile Rubbers (ilNBR), Chloroprene rubber (CR), polych!oroprene, Neoprene, EPM (ethylene propylene rubber, a copolymer of ethylene and propylene), Epichlorohydrin rubber (ECO), Polyacrylic rubber (ACM, ABR), Silicone rubber (SI, Q, VMQ), Fluorosilicone Rubber (FVMQ),
  • Natural rubber NR.
  • Synthetic polyisoprene IR
  • Butyl rubber copolymer of is
  • Fluoroelastoiners Viton, Tecnoflon, Fluorel, Aflas,
  • FFKM Perfluoroelastomers
  • PEBA Poly ether block amides
  • CSM Ch!orosu!fonated polyethylene
  • EVA Ethylene-vinyl acetate
  • TPE Thermoplastic elastomers
  • TPO Thermoplastic olefins
  • resilin elastin and Polysulfide rubber.
  • plastic material to be employed in the use or method as described herein may be an organic polymer selected from the group of polyethylene, polypropylene, polystyrene, polycarbonate and polycyeloolefin.
  • Polyethylene refers to a polymeric material composed of long chains of the monomer ethylene. Polyethylene material may be present in different forms of density and/or branching. Examples of polyethylene material include Ultra high molecular weight polyethylene (UHMWPE), i.e. a polyethylene with a molecular weight of between about 3.1 and 5.67 million and densities of about 0.930-0.935 g/cm 3 ; Ultra low molecular weight polyethylene (ULMWPE or PE- WAX); High molecular weight polyethylene (HMWPE); High density polyethylene (HDPE), i.e. a polyethylene with a density of greater or equal to 0.941 g/cm 3 .
  • UHMWPE Ultra high molecular weight polyethylene
  • ULMWPE or PE- WAX Ultra low molecular weight polyethylene
  • HMWPE High molecular weight polyethylene
  • HDPE High density polyethylene
  • High density cross-linked polyethylene HDXLPE
  • Cross- linked polyethylene PEX or XLPE
  • MDPE Medium density polyethylene
  • LLDPE Linear low density polyethylene
  • a polyethylene with a density range of 0.915-0.925 g/cm 3 which is a substantially linear polymer with significant numbers of short branches, commonly made by copolymerization of ethylene with short-chain alpha-olefins
  • Very low density polyethylene (VLDPE), i.e. a polyethylene with a density range of 0.880-0.915 g/cm 3 which is a substantially linear polymer with high levels of short-chain branches, commonly made by copolymerization of ethylene with short-chain alpha-olefins.
  • Polypropylene refers to a thermoplastic polymer composed of monomeric propylene units.
  • examples of polypropylene include homopolymer polypropylene, random copolymer polypropylene, and block copolymer polypropylene.
  • Propylene may also comprise polypropylene derivatives comprising units of polypropylene and ethylene or polyethylene units.
  • Polystyrene as used herein refers is an aromatic polymer made from the aromatic monomer styrene. Examples of polystyrene include isotactic polystyrene, atactic polystyrene and syndiotactic polystyrene.
  • Polycarbonate refers to thermoplastic polymers comprising carbonate groups. Polycarbonates may be derived from a combination of bisphenol A and phosgene, a transestrification of bisphenol A and diphenyl carbonate.
  • Polycarbonate material may in one embodiment be transparent.
  • Polycycloolefine refers to of alkene hydrocarbons, which contain more than one closed ring of carbon atoms, but have no aromatic character.
  • Polycycloole ines may, for example, be composed of monomeric alkenes such as cyclopropene, cyclobutene, cyclopentene, cyclohexene, cycloheptene, 1 ,3- cyclohexadiene, 1 ,4-cyclohexadiene or 1 ,5-cyclooctadiene.
  • the material is material suitable for the production of optical instruments, e.g. lenses, eyeglasses, sunglasses, contact lenses etc.
  • plastic materials with a high refraction index examples of such material are materials with a high refraction index, e.g. plastic materials with a high refraction index.
  • the group of plastic materials suitable for the production of optical instruments comprises, for example, polycarbonate plastics such as polyailyldiglycoicarbonat (PADC) or CR-39 or derivatives thereof.
  • PADC polyailyldiglycoicarbonat
  • plastic materials would be known to the person skilled in the art and/or can be derived from suitable, qualified textbooks, e.g. from Adolf Franck “Kunststoff-Kompendium”, Vogei, 6 th ed., 2006, which is incorporated herein in its entirety.
  • the material, e.g. plastic material may be any combination or juxtaposition of the above mentioned materials, or plastic materials.
  • the material, e.g. plastic material, to be transformed may comprise one or more additives.
  • An additive may, for example, be a pigment, dye or stain.
  • An example of such c lorant additives is carbon black.
  • Colorant additives may be present in the material, e.g. plastic material in any suitable amount, for example in an amount of about 0.001 % to about 25%.
  • a further additive which may be present in material, e.g. plastic material, to be transformed, is a lasersensitive compound.
  • laser sensitive compound refers to compounds, which are capable of absorbing a higher amount of laser radiation than neighbouring material, leading to locally increased temperatures and subsequent modifications as described herein in said regions or points.
  • Examples of laser sensitive compounds are nanoparticles of a diameter of about 5 nm to 300 nm in at least one dimension, e.g. of a diameter of about 100 nm in at least one dimension.
  • Lasersensitive compounds may be composed of one or more metals or alloys, e.g. nanoparticles comprising such metals or alloys.
  • nanoparticles may be present in a range of about 0.01 to about 10% of the material, e.g. plastic material.
  • a further additive which may be present in material, e.g. plastic material, to be transformed, may be a lacquer, e.g. a superficially applied lacquer.
  • the lacquer may be in a different color than the material, e.g. plastic material, and/or may convey different properties in comparison to the material underneath.
  • the lacquer may have a different transmissibi!ity for laser radiation, a different wetability, electrical conductivity or electrical chargeability.
  • the material e.g. plastic material may be covered or coated by biological or biochemical compounds, e.g. peptides, proteins, antibodies, nucleic acids, cell portions or fragments, cells, viral fragments etc.
  • biological or biochemical compounds e.g. peptides, proteins, antibodies, nucleic acids, cell portions or fragments, cells, viral fragments etc.
  • a further additive, which may be present in material, e.g. plastic material, to be transformed is a filler material.
  • filler material include glass, graphite, Si0 2 or Fe 2 0 3 .
  • the material, e.g. plastic material, to be transformed may be composed of more than one layer, e.g. 2, 3, 4, 5, 6, 7, 9 or 10 layers.
  • the layers may be of different physical composition, different color, different laser radiation transmissibility, different structure, different chemical composition or different durability.
  • the superficial layer may be composed o a transparent material, e.g. a transparent plastic material.
  • Such a material may additionally or alternatively, also have a high transmissibility for laser radiation.
  • the layer underneath may have a nontransparent form and/or comprise lasersensitive compounds, e.g. nanoparticlcs as described herein. Upon application of laser radiation a modification of the material may only take place in the non-superficial layer.
  • the laser radiation to be applied within the method or uses as described herein comprises the application of a specific amount of energy per area of the treated material, e.g. plastic material.
  • area of treated material means the zone or area of material in which the laser radiation impinges. This area excludes neighboring zones or regions, in which no laser radiation impacts.
  • the amount of energy may be between about 0.05 nJoule/ ⁇ 2 to about 150 treated material, e.g. plastic material. In one embodiment, the amount of energy may be between about 0.1 nJoule/ ⁇ 2 to about 100 nJoule/nnftreated material, e.g. plastic material, e.g.
  • the energy may be at about 150 nJouIe/ ⁇ 2 treated material.
  • the amount of energy to be applied may adapted to the material used, the type of modification envisaged, the laser radiation source used, the laser type used, the laser model used or any other suitable parameter known to the person skilled in the art.
  • the laser radiation is a laser radiation of a wavelength of about 355 nm to about 1064 nm.
  • the laser radiation may, for example, be of wavelength of about 355 nm to about 500 nm, or of about 500 nm to about 1064 nm.
  • the laser radiation may, for instance, be of a wavelength typical for commercially available lasers, e.g.
  • the laser radiation is a radiation of about 131 nm.
  • suitable wavelengths and/or o suitable lasers to be employed can be derived from a qualified textbook, e.g. from Orazio Svelto: “Principles of Lasers", Springer, 4 th ed., 1998, which is incorporated herein in its entirety.
  • the laser radiation of about 355nm and/or 1064 nm may be obtained in one embodiment from a neodymium : yttrium aluminium garnet (Nd:YAG) laser.
  • the optically modulating state of the material may absorb light in a wavelength spectrum of about 380 nm to about 540 nm and/or a wavelength spectrum of about 635 nm to about 655 nm.
  • the material may absorb light at a wavelength of about 380 nm, 390 nm, 400nm, 410 nm, 420 nm, 430 nm, 440 nm, 450 nm, 460 nm, 470 nm, 480 nm, 490 nm, 500 nm, 510 nm, 520 nm, 530 nm, 540 nm, and/or 630 nm, 635 nm, 640 nm, 645 nm, 650 nm, 655 nm or 660 nm.
  • the modified materia! may absorb light in a wavelength spectrum of about 510 nm to about 530 nm.
  • the modified material may absorb light at a wavelength of about 500 nm, 5 10 nm, 520 nm, 530 nm or 540 nm.
  • the modi ied material may further absorb light at more than one wavelength, e.g. at two or more of the above indicated wavelengths.
  • the optically modulating state of the plastic material may emit upon excitation, e.g. upon an excitation as described above, light in a wavelength spectrum of about 550 nm to about 800 nm.
  • the material may emit upon excitation light at a wavelength of about 540 nm, 550 nm, 560 nm, 570 nm, 580 nm, 590 nm, 600 nm, 610 nm, 620 nm, 630 nm, 640 nm, 650 nm, 660 nm, 670 nm, 680 nm, 690 nm, 700 nm, 710 nm, 720 nm, 730 nm, 740 nm, 750 nm, 760 nm, 770 nm, 780 nm, 790 nm, 800 nm, or 810 nm.
  • the modified material may emit upon excitation light at a wavelength of about 593 nm. In a further embodiment, the modified materia! may emit upon excitation light at a wavelength of about 685 nm. In a further embodiment, the modified material may emit upon excitation light at a wavelength spectrum of about 560 nm to about 660. In a further embodiment, the modified material may emit upon excitation light at a wavelength spectrum of about 660 nm to about 700 nm. The modified material may further emit upon excitation light at more than one wavelength, e.g. at two or more of the above indicated wavelengths.
  • the modified material may upon excitation at a wavelength of about 510 nm to about 530 nm emit light at a wavelength of about 560 to 600 nm and/or 660 to 700 nm.
  • the optically modulating state of the plastic material may emit upon excitation light at peak wavelengths of 593 nm and/or 685 nm.
  • peak wavelength as used herein means a wavelength point around which light emission in a broader spectrum occurs.
  • the transformation of the material e.g. plastic material, may comprise the generation of optically modulating elements or figures. In one embodiment the optically modulating elements may be generated on the surface of said plastic material.
  • optically modulating elements may be generated on in a non-surface layer of the material, e.g. a deeper layer of said plastic material.
  • optically modulating element or “element” as used herein refers to any kind of geometrical form, pattern or picture. Examples of such elements include a spot, dot, line, circle, square, character, a string or combination of characters, any type of symbol or string or combination of symbol. Further envisaged are a drawings, a barcode a datamatrix or a datamatrix code, or any combination of the mentioned elements.
  • An optically modulating element may also have a three dimensional form, e.g. a relief form. Such three dimensional forms may be present at surface layers of the material or in deeper layers of the material.
  • the optically modulating element may have a diameter in at least one dimension of at least about 5 ⁇ .
  • the element may have a diameter in at least one dimension of at least about 5 ⁇ , 6 ⁇ , 7 ⁇ , 8 ⁇ , 10 ⁇ , 12 ⁇ , 15 ⁇ , 20 ⁇ , 30 ⁇ , 40 ⁇ , 50 ⁇ , 75 ⁇ or 100 ⁇ .
  • the elements may be present in a density of about 1000 to about 40000 elements per mm 2 .
  • the density may be about 1000, 5000, 10000, 20000, 30000, 35000, 40000 elements per mm 2 .
  • the average distance between the elements may be about
  • the elements may be separate elements.
  • the elements may be joined elements. "Joined elements" may, for example, comprise a conjunction of neighboring spots forming a line, circle, square, character, symbol etc. Such joined elements may also comprise or be composed of continuous forms obtained by the application of laser radiation as defined above, e.g. grooves or prolonged craters or cuts within the transformed material, e.g. plastic material.
  • the material e.g. plastic material
  • the material, e.g. plastic material may be transparent.
  • the material, e.g. plastic material may comprise a transparent layer.
  • such transparent material may be composed of or comprise polycarbonate plastics or layers made of polycarbonate plastics.
  • the transparent material may in a further embodiment comprise lasersensitive compounds as defined herein, e.g. nanoparticles.
  • the transformed material e.g. plastic material, i.e. the material being transformed into an optically modulating state may be water- resistant and/or water indissoluble, or be resistant to or indissoluble in other liquids or aqueous solutions.
  • a water-resistant transformed material, e.g. plastic material may, for example, be useful for applications in wet, aqueous or liquid environments, e.g. in micro fluidic devices or cartridges etc.
  • water indissoluble material e.g. plastic material, may for instance be useful in wet, aqueous or liquid environments, e.g. in microfiuidic devices or cartridges etc.
  • a water-resistant or water indissoluble transformed material may be used for focusing procedures in wet, aqueous or liquid environments; for detection, qualification and/or quantification processes in wet, aqueous or liquid environments; for optical adjustments in wet, aqueous or liquid environments; and/or for in situ detection, qualification and/or quantification processes in liquid probe or sample environments, e.g. in blood, serum, urine, saliva, lymph etc. samples.
  • Corresponding environments may be present or generated, for example, in microfluidic devices, cartridges, reaction chambers or derivatives or subforms thereof, e.g. in devices, cartridges, systems or reactions chambers as described herein.
  • the transformed material e.g. plastic material, i.e. the material being transformed into an optically modulating state keeps its optical properties in a wet, aqueous or liquid environment, e.g. in solvents.
  • the transformation method works in particular without the necessity of using solvents, e.g. organic solvents, for printing or marking purposes.
  • the transformed material may be persistant to solvents or liquids which are capable of removing superficially applied colors or dyes.
  • optically modulating material may be produced by a method as defined herein.
  • Optically modulating material may be obtained with, be obtainable by or be produced by a method for the transformation of material, e.g. plastic material, as defined herein.
  • the optically modulating material e.g. plastic material
  • obtained with, obtainable by or produced by a method for the transformation of material, e.g. plastic material, as defined herein comprises a datamatrix of optically modulating elements.
  • a "datamatrix" as used herein may comprise a one or two- dimensional matrix barcode, e.g. consisting of or comprising optically distinguishable fields or modules arranged in different forms, e.g. as squares or rectangular pattern.
  • the information to be encoded may be any suitable information, e.g. text, raw data, images, pictograms etc. For example, information on a device type, manufacturing date, manufacturing lot, spatial properties of the apparatus, component, device, cartridge etc.
  • encoded information may relate to physiochemical properties of an apparatus, component, device, cartridge etc. Such properties include, for example, analytes for which devices or test zones are configured to assay. Other properties include the identity and properties of reagents stored in the device and date information (e.g., the expiration date) of the device.
  • a data size from a few bytes up to 2 kilobytes or more may be used.
  • the length of the encoded data may be made dependent on the symbol dimension used.
  • error correction codes may be added to increase symbol strength.
  • the optically modulating material e.g. plastic material
  • the optically modulating material may comprise one or more datamatrixes wherein the datamatrix may be composed of optically modulating spots.
  • the optically modulating material e.g. plastic material
  • the optically modulating material may comprise one or more datamatrixes wherein the datamatrix may be composed of optically modulating dots, lines, symbols, fields, circles, squares, geometric forms, or combinations thereof.
  • the spots, lines or other geometric forms may, for example, be positioned in short distance to each other in order to provide the optical effect of squares or rectangular pattern.
  • optically modulating material e.g. plastic material
  • reference mark refers to a fiducial mark of any suitable size or shape.
  • An exemplary shape is a cross, a typical character, a drawing or the like.
  • a reference mark may also be in the form of a line, a rectangle, a dot etc.
  • a reference mark may, for example, be detected on the material, e.g. plastic material, during optical recognition processes, focusing processes, alignment processes, positioning processes etc. carried out on the material.
  • a reference mark or fiducial mark in one embodiment, may be employed for the alignment of arrays of elements, for the alignment of components of such arrays or for determination of the layout of probes on the array.
  • An example of an array is a micro-array.
  • a "micro-array” as used herein may include a certain material, such as a probe material, which may, for example, have an increased binding affinity for a target material, immobilized to a plurality of distinct regions on a substrate.
  • the regions may comprise at least one spot, and generally, at least two spots or regions are arranged on the substrate with an interval separating them or without an interval separating them.
  • the probe material may include a biomaterial, such as deoxyribonucleic acid ("DNA”), ribonucleic acid (“RNA”), complementary DNA (“cDNA”), messenger RNA (“mRNA”), protein, sugar or other similar materials.
  • Exemplary embodiments of the substrate may be formed of glass, silicon, plastic, ceramic, quartz or other materials with similar characteristics.
  • a reference mark e.g. in the form of a line, a rectangle, a dot, or any other marking as described herein, e.g. a figure, symbol, character etc. may be present in or on a material in conjunction with a micro-array as defined above.
  • a micro-array may be accompanied or surrounded by such reference marks or markings.
  • the micro-array is on the same surface as the reference marks.
  • the micro-array is on a different surface in comparison to the reference marks.
  • the micro-array may be mounted i a spatially defined manner with respect to the reference marks.
  • the micro-array itself may comprise a reference mark or marking as described herein, e.g. comprise regions, geometric elements, symbols, characters etc. composed of optically modulating material as described herein.
  • material e.g. plastic material, comprising optically modulating reference marks as described herein m y thus be used for the production, manufacture or generation of substrates, casings, devices, cartridges, systems or components thereof etc. comprising a micro-array.
  • substrates, casings, devices, cartridges, or systems may, for example, be identified, aligned, positioned, repositioned and/or calibrated based on the presence of the reference mark.
  • the calibration may in specific embodiments be a qualitative calibration, e.g. based on the presence and/or position and/or wavelength of emitted light of a reference mark.
  • the calibration may in specific embodiments be a quantitative calibration, e.g.
  • the emitted light may have a wavelength different from the wavelength emitted from markers used on the array, e.g. optical markers used on micro-arrays comprising DNA, RNA, proteins etc.
  • material e.g. plastic material, comprising optically modulating elements as described herein may be used as a fluorescence standard for validating and/or calibrating optical readers, systems or instruments capable of detecting the light emitted from the reference mark.
  • the validation and/or calibration may be performed based on the presence and/or position and/or wavelength and/or intensity and/or size of emitted light of an optically modulating element.
  • a method comprises the application of laser radiation to a material for marking the surface of the material, wherein the marked surface is optically modulating.
  • marking the surface refers to the generation of spots, areas or other geometrical elements or forms on said surface, which are distinguishable from their surrounding(s). This distinction includes at least an optical excitability of the marked surface, which is not present in the surroundings of the marked surface.
  • Optical excitability refers to an optically modulating state as defined herein. In one embodiment the optical excitability may be similar to a fluorescence, or be a fluorescent like state of the marked surface such as the emission of radiation at a wavelength different from the excitation wavelength as described herein.
  • “Surface” as used herein refers to the outermost layer of material, e.g. plastic material.
  • the surface may be of any roughness or shape and/or may be planar, or comprise crates, grooves or other structural modifications. In some embodiments, the surface may not only encompass the outermost layer of a material, but also a layer underneath, e.g. in materials comprised of various layers, for instance various thin layers.
  • the laser radiation to be employed in the method for marking the surface o a material comprises in some embodiments the application of an amount of energy of about 0.05 nJoule. ⁇ m 2 to about 150 ⁇ / ⁇ 2 treated surface or per single element/spot. In a further embodiment the amount of energy may be between about 0.05 nJoule/ ⁇ 2 to about 100 ⁇ / ⁇ 2 treated surface or per single element/spot, e.g.
  • the energy may be at about 1 10 nJoule/ m 2 , 150 nJoule/ ⁇ 2 treated material or per single element/spot.
  • the amount of energy may be provided in the form of laser radiation pulses.
  • Examples of application times for the pulses are ranges of about 0.05 ⁇ to 10 ms, 0.1 ⁇ to 5 ms, 1 ⁇ to 1 ms, or pulses of 2 ⁇ , 3 ⁇ , 4 ⁇ , 5 ⁇ , 6 ⁇ , 7 8, 8 ⁇ , 9 ⁇ , 10 ⁇ , 20 ⁇ , 30 ⁇ , 50 ⁇ , 100 ⁇ , 200 ⁇ , 300 ⁇ , 400 ⁇ , 500 ⁇ , 600 ⁇ , 700 ⁇ , 800 ⁇ , 900 ⁇ , 1 ms.
  • the amount of energy to be applied may be adapted to the material used, the surface structure, the surface material, the type of modi fication envisaged, the laser radiation source used, the laser type used, the laser model used or any other suitable parameter known to the person skilled in the art.
  • the laser types, the wavelength of the laser radiation to be employed and further parameters etc. are described herein above.
  • the optical excitation of the marked surface is a broadband light excitation.
  • Broadband light excitation as used herein relates to an excitation over a broad range of the visible and near-visible light spectrum, e.g. from about 400 nm to about 700 nm.
  • the optical excitation of the marked surface is an excitation in a wavelength spectrum of about 380 nm to about 540 nm and/or a wavelength spectrum of about 635 nm to about 655 nm
  • the marked surface may absorb light at a wavelength of about 380 nm, 390 nm, 400 nm, 410 nm, 420 nm, 430 nm, 440 nm, 450 nm, 460 nm, 470 nm, 480 nm, 490 nm, 500 nm, 510 nm, 520 nm, 530 nm, 540 nm, and/or 630 nm, 635 nm, 640 nm, 645 nm, 650 nm, 655 nm or 660 nm.
  • the marked surface may emit upon excitation, e.g. upon an excitation as described above, light in a wavelength spectrum of about 550 nm to about 800 nm.
  • the marked surface may emit upon excitation light at a wavelength of about 540 nm, 550 nm, 560 nm, 570 nm, 580 nm, 590 nm, 600 nm, 610 nm, 620 nm, 630 nm, 640 nm, 650 nm, 660 nm, 670 nm, 680 nm, 690 nm, 700 nm, 710 nm, 720 nm, 730 nm, 740 nm, 750 nm, 760 nm, 770 nm, 780 nm, 790 nm, 800 nm, or 810 nm.
  • the marked surface may emit upon excitation light at a wavelength of about 593 nm. In a further embodiment, the marked surface may emit upon excitation light at a wavelength of about 685 nm. In a further embodiment, the marked surface may emit upon excitation light at a wavelength spectrum of about 560 nm to about 660. In a further embodiment, the marked surface may emit upon excitation light at a wavelength spectrum of about 660 nm to about 700 nm. The marked surface may further emit upon excitation light at more than one wavelength, e.g. at two or more of the above indicated wavelengths. In a further embodiment, the marked surface may upon excitation at a wavelength of about 10 nm to about 530 nm emit light at a wavelength of about 560 to 600 nm and/or 660 to 700 nm.
  • the marked surface may emit upon excitation light at peak wavelengths of 593 nm and/or 685 nm.
  • a method comprises the production of an apparatus, device, micro fluidic device, cartridge, reaction chamber, object or utility or instrument, wherein said production comprises the employment of optically modulating materia! as component for said apparatus, device, microfluidic device, cartridge, reaction chamber, object of utility or instrument as described herein.
  • a method comprises the production of an optical instrument such as a lense, eyeglasses, sunglasses, a contact lense, a camera, an optical detection apparatuses etc. or components thereof, wherein optically modulating material as described herein is used as starting material, intermediate material or as component of the instruments.
  • a method comprises the production of an object of utility, e.g.
  • a method for the production of an apparatus, device, microfluidic device, cartridge, reaction chamber or instrument comprises one or more steps wherein the material, e.g. plastic material, of the apparatus, device, microfluidic device, cartridge, reaction chamber, object of utility or instrument or of one or more components thereof is transformed into an optically modulating state as defined herein.
  • apparatuses, devices, microfluidic devices, cartridges, reaction chambers, objects of utility or instruments e.g. optical instruments such as lenses, eyeglasses, sunglasses, contact lenses, cameras, optical detection apparatuses or components thereof, or objects of utility, e.g. a straw, tableware, a can, a box, a bottle, which comprise optically modulating elements, e.g. geometrical elements, characters, figures, codes, datamatrixes, or three dimensional forms such as holograms or reliefs, may accordingly be provided.
  • material comprising a marked surface comprising a marked surface, wherein said marked surface is optically modulating, may be produced by a method for marking the surface of a material as defined herein.
  • Material may be obtained with, obtainable by or produced by a method for marking the surface of a material as described herein.
  • the material comprising a marked surface may be a plastic material.
  • the material may also be of a combination of a non-plastic material and a plastic material, e.g. a composite material comprising a plastic surface and one or more a non-plastic layers.
  • non-plastic components may be metals, biological compounds such as proteins, peptides, nucleic acids, or derivatives thereof, silica, glass etc.
  • the plastic material may comprise non-plastic additives as described herein.
  • the plastic material may be a thermoplastic or elastomeric material as described herein above.
  • the plastic material may be an organic polymer selected from the group consisting of polyethylene, polypropylene, polystyrene, polycarbonate and polycycloolefin as described above.
  • material may comprise or be covered or at least partially be covered by a surface comprising one or more laser marks, wherein said laser mark is optically modulating.
  • Material may thus comprise or be covered or be at least partially covered by a surface comprising one or more laser marks, wherein said laser mark is optically modulating.
  • the term "one or more" as used herein refers to at least one laser mark, 2 laser marks, 3, 4, 5, 6, 7, 8, 9, 10, 20, 30, 40, 50, 60, 70, 80, 90, 100, 200.
  • laser mark refers to a spot, area or other shape or form on the surface of a material, which is obtained by the application of laser radiation.
  • a mark may be a single element or a conjunction or array of single marks.
  • a laser mark is typically distinguishable from the surrounding surface.
  • It may, for example, comprise a region or point of ablation, a crate in a planar or quasi planar surface, a scratch in a planar or quasi planar surface, a hole in a planar or quasi planar surface, an embossment in a planar or quasi planar surface, a rim of material in a planar or quasi planar surface, or a planar or quasiplanar region or point in a differently structured surface, e.g. in a rough surface, or in a surface comprising protrusions or
  • a laser mark as described herein is optically modulating as defined herein above.
  • the laser mark on the surface of a material is obtained from the application of laser radiation of an energy of about 0.05 nJoule/ ⁇ 2 to about 150 ⁇ / ⁇ 2 treated surface.
  • the amount of energy may be between about 0.05 nJoule/ ⁇ ' to about 100 ⁇ / ⁇ 2 treated surface or per single element/spot, e.g. in a range of about 0.5 nJoule/ ⁇ 2 to about 0 ⁇ / ⁇ 2 , a range of about 10 nJoule/ ⁇ 2 to about 25 ⁇ / ⁇ 2 , a range of about 0,1 ⁇ 1 ⁇ 1 ⁇ / ⁇ ⁇ 2 to about 20 nJoule/ ⁇ 2 , a range of about O.
  • the energy may be at about 1 nJoule/ ⁇ 2 , 5 n.Ioule/um 2 , 10 nJoule/ ⁇ ) 2 , 150 nJoule/ ⁇ 2 treated material or per single element/spot.
  • the amount of energy to be applied may be adapted to the surface form, structure or the material of the surface, the type of modification envisaged, the laser radiation source used, the laser type used, the laser model used or any other suitable parameter known to the person skilled in the art.
  • the laser mark may emit upon excitation, e.g. upon an excitation as described above or below, light in a wavelength spectrum of about 550 nm to about 800 nm.
  • the laser mark may emit upon excitation light at a wavelength of about 540 nm, 550 nm, 560 nm, 570 nm, 580 nm, 590 nm, 600 nm, 610 nm, 620 nm, 630 nm, 640 nm, 650 nm, 660 nm, 670 nm, 680 nm, 690 nm, 700 nm, 710 nm, 720 nm, 730 nm, 740 nm, 750 nm, 760 nm, 770 nm, 780 nm, 790 nm, 800 nm, or 810 nm.
  • the laser mark may emit upon excitation light at a wavelength of about 593 nm. In a further embodiment, the laser mark may emit upon excitation light at a wavelength of about 685 nm. In a further embodiment, the laser mark may emit upon excitation light at a wavelength spectrum of about 560 nm to about 660. In a further embodiment, the laser mark may emit upon excitation light at a wavelength spectrum of about 660 nm to about 700 nm. The laser mark may further emit upon excitation light at more than one wavelength, e.g. at two or more of the above indicated wavelengths. In a further embodiment, the laser mark may upon excitation at a wavelength of about 5 10 nm to about 530 nm emit light at a wavelength of about 560 to 600 nm and/or 660 to 700 nm.
  • the laser mark may emit upon excitation light at peak wavelengths of 593 nm and/or 685 nm.
  • the optical excitation of the laser mark is a broadband light excitation as described herein above.
  • the optical excitation of the laser mark is an excitation in a wavelength spectrum of about 380 nm to about 540 nm and/or a wavelength spectrum of about 635 nm to about 655 nm.
  • the laser mark may absorb light at a wavelength of about 380 nm, 390 nm, 400 nm, 410 nm, 420 nm, 430 nm, 440 nm, 450 nm, 460 nm, 470 nm, 480 nm, 490 nm, 500 nm, 510 nm, 520 nm, 530 nm, 540 nm, and/or 630 nm, 635 m, 640 nm, 645 nm, 650 nm, 655 nm or 660 nm.
  • the material comprising a surface comprising one or more laser marks is a plastic material.
  • the material may also be of a combination of a non-plastic material and a plastic material, e.g. a composite material comprising a plastic surface and one or more a non-plastic layers.
  • non-plastic components may be metals, biological compounds such as proteins, peptides, nucleic acids, or derivatives thereof, silica, glass etc.
  • the plastic material may comprise non-plastic additives as described herein.
  • the plastic material may be a thermoplastic or elastomeric material as described herein above.
  • the plastic material may be an organic polymer selected from the group consisting of polyethylene, polypropylene, polystyrene, polycarbonate and polycycloolefin as described herein above.
  • a datamatrix on a material may be composed of or comprise a laser mark, wherein said laser mark is optically modulating.
  • a datamatrix may be datamatrix as defined above, e.g. comprising a one or two-dimensional matrix barcode consisting of optically distinguishable fields or modules arranged in different forms, e.g. as squares or rectangular pattern.
  • the information to be encoded may be any suitable information, e.g. text, raw data, images, pictograms etc. For example, information on a device type, manufacturing date, manufacturing lot, spatial properties of the apparatus, component, device, cartridge etc. or sub-elements thereof, encountered peculiarities during quality checks, the amount, size, position etc. of comprised elements or components etc. may be encoded.
  • encoded information may relate to physiochemical properties of an apparatus, component, device, cartridge etc.
  • properties include, for example, analytes for which devices or test zones are configured to assay.
  • Other properties include the identity and properties of reagents stored in the device and date information (e.g., the expiration date) of the device.
  • the material on which the datamatrix is located can be a plastic material, e.g. a plastic material as defined herein above.
  • material may also include an apparatus, a device, a cartridge, a reaction chamber, a microfluidic device, or reaction zone being present in such entities, or any component thereof or any combination thereof.
  • the laser mark of the datamatrix may emit upon excitation, e.g. upon an excitation as described herein, light in a wavelength spectrum of about 550 nm to about 800 nm as described herein above.
  • the laser mark of the datamatrix may emit upon excitation light at peak wavelengths of 593 nm and/or 685 nm as described herein above.
  • the optical excitation of the laser mark of the datamatrix may be a broadband light excitation as described herein above.
  • the optical excitation of the laser mark of the datamatrix may be an excitation in a wavelength spectrum of about 380 nm to about 540 nm and/or a wavelength spectrum of about 635 nm to about 655 nm as described herein above.
  • the datamatrix may be composed of optically modulating laser marks, which form, comprise or are geometric forms, geometric pattern, spots, dots, lines, squares, circles, characters, symbols, drawings, barcode or any combination thereof.
  • conjunctions of datamatrixes on a material as defined above are also envisaged, e.g. datamatrixes encoding different types of information being located in different sections of a device or apparatus, or in different reaction zones of such entities.
  • a reference mark on a material may be composed of or comprise a laser mark, wherein said laser mark is optically modulating.
  • a reference mark may be reference mark as defined above, e.g. a fiducial mark of any suitable size or shape, such as a cross, a character, a drawing or the like.
  • a reference mark may also be in the form of a line, a rectangle, a dot etc.
  • a reference mark may, for example, be detected on the material, e.g. plastic material, during optical recognition processes, focusing processes, alignment processes, positioning processes etc. carried out on the material.
  • the material on which the reference mark is located can be a plastic material, e.g. a plastic material as defined herein above.
  • the material on which the reference mark is located may also include an apparatus, a device, a cartridge, a reaction chamber, a microfluidic device, or reaction zone being present in such entities, or any component thereof or any combination thereof.
  • the laser mark of the reference mark may emit upon excitation, e.g. upon an excitation as described herein, light in a wavelength spectrum of about 550 nm to about 800 nm as described herein above.
  • the laser mark o the reference mark may emit upon excitation light at peak wavelengths of 593 nm and/or 685 nm as described herein above.
  • the optical excitation of the laser mark of the reference mark may be a broadband light excitation as described herein above.
  • the optical excitation of the laser mark of the reference mark may be an excitation in a wavelength spectrum of about 380 nm to about 540 nm and/or a wavelength spectrum of about 635 nm to about 655 nm as described herein above.
  • the reference mark on a material may be an alignment mark.
  • alignment mark refers to a mark suitable for identifying a target position or region or sector in a material, e.g. a device, cartridge, casing, reaction chamber etc., and/or for allowing focusing procedure on said marking, and/or for allowing a positing or repositioning action of an interacting device or apparatus or reader or components thereof with the entity comprisin the alignment mark.
  • Such a positioning or repositioning action may, for example, comprise the decrease or increase of angles or inclinations between an alignment mark and interacting device or apparatus or reader or components thereof.
  • Alignment marks also can include physical structures like microstructures and the like.
  • the reference mark on a material may be an array alignment mark.
  • array alignment mark refers to a mark suitable for identifying a target position or region or sector in on a reaction chamber, cartridge, or casing comprising an array, e.g. an micro-array as described above, or on the array itself or the underlying substrate or material; and/or suitable for allowing a focusing procedure on said marking; and/or suitable for allowing a positioning or
  • a positioning or repositioning action of an interacting device or apparatus or reader or components thereof with the entity comprising the alignment mark may, for example, comprise the decrease or increase of angles or inclinations between the array alignment mark and the interacting device or apparatus or reader or components thereof.
  • the action may, for example be carried out by optical readers or instruments capable of detecting the light emitted from the reference mark.
  • the emitted light may have a wavelength different from the wavelength emitted from markers used on the array, e.g. optical markers used on micro-arrays comprising DNA, RNA, proteins etc.
  • optically- modulating material or material comprising a laser mark or marking or a marked surface, wherein said mark or marking or marked surface is optically modulating may be used for the manufacture or production of an apparatus, device, microfiuidic device, cartridge, reaction chamber, object of utility or instrument, or may be used as component for the manufacture or production of an apparatus, device, microfiuidic device, cartridge, reaction chamber, object of utility or instrument.
  • Manufacture or production details and/or processes are known to the person skilled in the art.
  • Examples of devices, apparatuses, microfiuidic devices etc., which may be manufactured with the material as defined herein, as well as processes for the their production or manufacture can be derived from Fundamentals and Applications of Microlluidics, Nam-Trung Nguyen, Steve Wereley, 2002, Artech House Publishers; 1 st ed; or in Microsystem Engineering of Lab-on-a-Chip Devices, Oliver Gerike et al. t 2008, Wiley-VCH; 2 nd edition, which are incorporated by reference in their entirety.
  • Examples of instruments for whose manufacture material as described herein may be used comprise optical instruments such as lenses, eyeglasses, sunglasses, contact lenses, cameras, optical detection apparatusses or components thereof etc.
  • Examples of objects of utility for whose manufacture material as described herein may be used comprise a straw, tableware, a can, a box or a bottle or components thereof etc.
  • apparatuses, devices, microf!uidic devices, cartridges, objects of utility or instruments may comprise optically modulating spot elements, reference marks, geometric forms, marked surfaces, two or three dimensional forms etc. as described herein.
  • a method for the manufacture or production of an apparatus, device, micro fluidic device, cartridge, reaction chamber or components thereof comprises the step of transforming material or a part of the material of said apparatus, device, micro fluidic device, cartridge, reaction chamber into an optically modulating state the application of laser radiation to the material.
  • the transformation of material includes in one embodiment the application of laser radiation as define herein above. In another embodiment the transformed material is present in an optically modulating state, as defined herein above.
  • the material to be transformed is plastic material as defined herein above, e.g. thermoplastic material or elastomeric material as described herein.
  • the material may also be a combination of plastic material with other materials, e.g. metals, silica etc. as described herein.
  • Processes for the manufacture of a device besides the indicated transformation steps are known to the person skilled in the art and can, for example, be derived from Fundamentals and Applications of Microfluidics, Nam-Trung Nguyen, Steve Wereley, 2002, Artech House Publishers; 1 st ed; or in Microsystem Engineering of Lab-on-a-Chip Devices, Oliver Gerike et al., 2008, Wiley- VCH; 2 nd edition, which are incorporated by reference in their entirety.
  • the device obtained by the method of manufacture, or when using material as described herein is a device comprising a first channel having an inlet opening, and a longitudinal section in fluid communication with the inlet opening.
  • Material transformed into an optically modulating state may, for example, be used for the production or be present in the first channel, in or near the inlet opening, and/or at the longitudinal section in fluid communication with the inlet opening.
  • the device obtained by the method of manufacture, or when using material as described herein is a device comprising a first channel having an inlet opening, an outlet and a longitudinal section between said inlet and said outlet.
  • Material transformed into an optically modulating state may, for example, be used for the production or be present in the first channel, in or near the inlet opening, in or near the outlet opening, and/or at the longitudinal section between the inlet or outlet.
  • Further forms of the device or cartridge are also envisaged, e.g. devices wherein only an inlet port is present, i.e. self-contained devices or cartridges.
  • the device obtained by the method of manufacture, or when using material as described herein is a device which comprises a first channel having an inlet opening, an outlet, and a longitudinal section between said inlet opening and said outlet, a channel including a capillary inlet; and a detection region in fluid communication with the capillary inlet.
  • Material transformed into an optically modulating state may, for example, be used for the production or be present in the capillary inlet and/or the detection region, in or near the channel including the inlet or outlet.
  • Further forms of the device or cartridge are also envisaged, e.g.
  • the device obtained by the method of manufacture, or when using material as described herein is a device which comprises a first channel having an inlet opening, an outlet, and a longitudinal section between said inlet openin and said outlet, a channel including a capillary inlet: and a detection region in fluid communication with the capillary inlet; and a microfluidic flow path having an at least partially deformable wall and being in fluid communication with the detection region of the channel.
  • Material transformed into an optically modulating state may, for example, be used for the production or be present in the capillary inlet and/or the detection region, in or near the micro fiuidic flow path, in or near the channel including the inlet or outlet, and/or at the deformable wall section.
  • Further forms of the device or cartridge are also envisaged, e.g. devices wherein only an inlet port is present, i.e. self-contained devices or cartridges. Examples of such devices and further details are described in International Patent Application
  • the device obtained by the method of manufacture, or when using material as described herein is a device for qualitatively and/or quantitatively detecting molecular interactions between probe molecules and target molecules, comprising a micro-array comprising probe molecules immobilized in array elements, said micro-array being disposed on a first surface of the device; and a reaction chamber formed between the first surface including the micro-array disposed thereon, and a second surface.
  • Material transformed into an optically modulating state may, for example, be used for the production or be present in the first surface of the device, the reaction chamber formed between the first surface including the micro-array disposed thereon, and/or the second surface.
  • Further forms or derivatives of the device are also envisaged, e.g. devices wherein the micro-array may be disposed on the second surface. Examples of such devices and further details are described in International Patent Application WO 2005/108604 (which is incorporated by reference in its entirety).
  • the device obtained by the method of manufacture, or when using material as described herein is a device which comprises first and second substrates defining a channel therebetween, at least one of the substrates being flexible, the channel comprising an array of spaced-apart test zones, each test zone comprising a probe compound configured to participate in an assay for a target analyte.
  • Material transformed into an optically modulating state may, for example, be used for the production or be present in the channel between the first and second substrates, and/or on or in proximity to the test zones. Further forms or derivatives of the device are also envisaged. Examples of such devices and further details are described in International Patent Application WO 2008/062048 (which is incorporated by reference in its entirety).
  • the device obtained by the method of manufacture, or when using material as described herein is a device which comprises a reaction chamber formed within a chamber body between a first surface and a second surface.
  • Material transformed into an optically modulating state may, for example, be used for the production or be present in the first surface and/or second surface.
  • Further forms or derivatives of the device are also envisaged, e.g. devices wherein the first surface comprises a micro-array and/or wherein the distance between the micro-array and the second surface is variable.
  • the device obtained by the method of manufacture, or when using material as described herein is a device which comprises a reaction chamber formed within a chamber body between a first surface and a second surface, wherein the second surface is located opposite to the first surface, wherein the distance between the first surface and the second surface is variable at least in one or more parts of the surface area of the first surface and/or the second surface.
  • Material transformed into an optically modulating state may, for example, be used for the production or be present in the first surface and/or second surface.
  • Further forms or derivatives of the device are also envisaged, e.g. devices wherein the first surface comprises a micro-array and/or wherein the distance between the micro-array and the second surface is variable.
  • the device obtained by the method of manufacture, or when using material as described herein is a device which comprises a reaction chamber formed within a chamber body between a first surface and a second surface, wherein the second surface is located opposite to the first surface; and one or more displacers, wherein the distance between the first surface and the second surface is variable via the one or more displacers at least in one or more parts of the surface area of the first surface and/or the second surface.
  • Material transformed into an optically modulating state may, for example, be used for the production or be present in the first surface and/or second surface and/or in or on the displacer. Further forms or derivatives of the device are also envisaged, e.g.
  • the first surface comprises a micro-array and/or wherein the distance between the micro-array and the second surface is variable and wherein the second surface has a displacement structure and/or wherein the displacer or displacement structure is not part of the device, but provided by an external entity. Examples of such devices and further details are described in International Patent Application WO 2007/05 1863 (which is incorporated by reference in its entirety).
  • the device obtained by the method of manufacture, or when using material as described herein is a device or derivative thereof as described, for example, in International Patent Application WO 2008/055915 or WO 2009/013321 , which are incorporated by reference in their entirety.
  • the device obtained by the method of manufacture, or when using material as described herein is a device comprising a first channel having an inlet opening, and a longitudinal section in fluid communication with the inlet opening; and a control element.
  • the device obtained by the method of manufacture, or when using material as described herein is a device comprising a first channel having an inlet opening, an outlet and a longitudinal section between said inlet and said outlet; and a control element.
  • the device obtained by the method of manufacture, or when using material as described herein is a device which comprises a cartridge having a microfluidic channel including a capillary inlet; and a detection region in fluid communication with the capillary inlet; a microfluidic flow path having an at least partially deformable wall and in fluid communication with the detection region of the channel; and a control element.
  • Material transformed into an optically modulating state may, for example, be used for the production or be present in the microfluidic channel, the capillary inlet, and/or the detection region, the microfluidic path, in the vicinity of the partially deformable wall and/or be present in or constitute a control element.
  • control element as used herein relates to a unit or factor or means which allows the testing, reviewing, examining, scanning, revising or inspecting of the device or sub-unit of the device or system or of a test result or a result of the analysis and also to the possibility to compare, verify and contrast obtained results during and/or after the use of a device or system or during and/or after performing the methods described herein.
  • the term also denotes the performance of such controlling activities.
  • Further forms or derivatives of the devices are also envisaged, e.g. devices additionally comprising a cap comprising a sealing member configured to seal with the inlet and form a fluid circuit including the inlet, the microfluidic channel and the microfluidic flow path. Examples of such devices and further details are described in International Patent Application WO 2008/135564.
  • optically modulating material or material comprising a laser mark or marking or a marked surface wherein said mark or marking or marked surface is optically modulating may be used for controlling optical parameters.
  • optical parameters refers to a parameter such as focus, area of an image, exposure time, distance between elements, turbidity etc. These parameters may be linked to the optical excitability of the material.
  • the optical modulation as defined herein of the material may be determined by taking images of the material. Differences of the optical modulation over time, differences of the optical modulation due to changes in intermediate spaces (e.g.
  • Controlling comprises one or more measurement steps for one or more of these parameters and a subsequent comparison with internal or external data, or with data obtained in subsequent or previous measurement steps.
  • the optical parameter which is to be controlled is the focus of an optical device or reading system.
  • a method comprises the checking or controlling of the focus of a detection unit of a system or associated with a device via said optical parameter.
  • the focus of a detection unit of a system or associated with a device wherein said system or device comprises or is composed of optically modulating material as described herein, e.g. present or located within a device, system, cartridge or microfluidic channel, may be checked and adjusted i necessary; comprising the steps of adjusting the exposure time for the detection unit; optically detecting an optically modulating element, spot, form etc.
  • determining a first value indicative for number of optically modulating elements, spot, form etc. in said area determining a second value indicative for the usability of the device or system and/or o any procedure, function or method carried out with or in said device or system, based on a comparison o the first value with a threshold value.
  • the checking of the focus of a detection unit is typically a comparison of one or more parameters with suitable threshold or predefined values.
  • Such parameters are the conversion of light from object points.
  • Such a conversion may, for instance, be determined by circle of confusion criteria as known to the person skilled in the art.
  • An object or image point may accordingly be considered as being in focus if light is converged almost as much as possible based on circle of confusion criteria.
  • these criteria are not met, the focus may be adjusted. This may be done automatically, e.g. with the help of electronic or mechanical devices, typically in the form of autofocussing on an object. Suitable techniques, devices, or calculation methods etc. are known to the person skilled in the art. Alternatively, the focus may be adjusted manually.
  • a detection unit may be comprised in a system, e.g. a system for performing assays such as biological, medical, chemical, biochemical assays, cell counting etc. or may be associated with a device wherein assays may be performed such as biological medical, chemical, biochemical assays, cell counting etc.
  • the detection unit may be comprised in a system or device as mentioned herein.
  • the detection unit may be associated with a device as mentioned herein.
  • the exposure time for the detection unit may be adjusted according to the amount and intensity of light reaching the detection unit, e.g. in reaction to the depth of image field, the distance range over which objects are acceptably sharp or in focus or any other suitable parameter known to the person skilled in the art.
  • the adjustment may be carried out automatically, e.g. with the help of electronic or mechanical devices, typically in the form of an automated comparison to a lookup table. Suitable techniques, devices, lookup tables for threshold values etc. are known to the person skilled in the art.
  • the exposure time may be adjusted manually.
  • a value indicative for the number of optically modulating elements, spots, forms etc. may be compared to a threshold value or lookup table. If, for example, the indicative number of such optically modulating elements, spots, forms etc. is zero, i.e. no optically modulating element, spot, form is detectable, the device or system and/or any procedure, function or method carried out with or in said device or system may be considered as non-usable. Alternatively, if, for example, the value indicative for the number of optically modulating elements, spots, forms is much larger than a predefined value or the threshold value, e.g. larger than 100.000, i.e.
  • the device or system and/or any procedure, function or method carried out with or in said device system may also be considered as non-usable. Otherwise, i.e. if the value is within a threshold range, e.g. as indicated above, the device or system and/or any procedure, function or method carried out with or in said device system may also be considered as usable and/or be confirmed.
  • a non-usability situation is encountered in this context the usage of the device or system may be discontinued and/or any results obtained may be disregarded.
  • Corresponding information may be recorded electronically or encoded in a barcode or any other suitable coding material.
  • a barcode may, for instance, be attached to a device or microfiuidic channel.
  • the adjustment reactions may be determined in reaction to the value indicative for the number of optically modulating, elements, spots, forms. If, for example, no optically modulating, elements, spots, forms are detected, the focus of the detection system may be adjusted or further adjusted if it was already adjusted before. In some embodiments, the adjustment may be accomplished by a variation of the distance between the detection system and a material comprising said optically modulating, elements, spots or forms, e.g. a microfluidic channel, e.g.
  • the exposure time may be adjusted or further adjusted if it was already adjusted before.
  • the exposure time may, for example, be increased or decreased by about 10, 20, 30, 50, 100, 200, 500, 1000 or 10.000%.
  • Such a modification may be reiterated one or several times, followed or preceded by the other method steps as described herein.
  • a reiteration of additional adjustments of the focus, predefined area and/or exposure time may be carried out for each of the parameters of focus, predefined area and exposure time independently or for a combination of parameters. Such a reiteration may be carried out for 1 to about 20 times, e.g. 2, 3, 4, 5, 6, 7, 8, 9, 10 times.
  • a comparison of a value indicative for the usability of the device or system is within a predefined range the device or system may be continued to be used and/or the results obtained or to be obtained with said device or system may be confirmed.
  • the methods may accordingly be carried out before or after carrying out an assay as described herein. Alternatively, the method may be carried out during the performance of an assay as described herein.
  • the steps of the method mentioned above may be carried out in a different order, e.g. first a value indicative for the number of optically modulating elements, spots, forms etc. in an area may be determined, subsequently a value indicative for the usability may be determined. If at this stage a non-usability situation is encountered the focus may be checked and/or adjusted and/or the exposure time may be adjusted and/or the area of optical detection may be adjusted as described herein.
  • the threshold value for controlling the focus position may be for instance the detection of minimum number of 3 optically modulating elements, spots or forms as lower limit and about 10.000 optically modulating elements, spots or forms as upper limit, for instance 5, 10, 50, 100 or 500 optically modulating elements, spots or forms.
  • the second value indicative for the usability of the device or system and/or of any procedure, function or method carried out with or in the device or system is a deviation of not more than 40%, 35%, 30%, 25%, 20%, 15%, 12%, 11%, 10%, 9%, 8%, 7%, 6%, 5%, 4%, 3%, 2% or 1% between the first value, i.e.
  • the test may be considered as being usable and/or any procedure, function or method carried out with or in the device or system may be confirmed. If a concomitant assay is carried out, corresponding images may be taken and/or recorded and/or further processed.
  • the second value indicative for the usability of the device or system and/or of any procedure, function or method carried out with or in the device or system is a deviation of more than about 40%, 35%, 30%, 25%, 20%, 15%, 12%, 1 1 %, 10%, 9%, 8%, 7%, 6%, 5%, 4%, 3%, 2% or 1% between the first value, i.e. the value indicative of the number of optically modulating elements, spots or forms in a predefined area o the device, cartridge or microfluidic channel and the threshold value of 3 optically modulating elements, spots or forms, or about 10.000 optically modulating elements, spots or forms, the test may be regarded as being non-usable.
  • the device or system may be regarded as non-usable and/or any procedure, function, test or method carried out with or in the device or system may be considered as inaccurate.
  • the test or usage of the device or system may accordingly be discontinued and/or the results obtained may be disregarded.
  • a microfiuidic device comprises a first channel having an inlet opening, and a longitudinal section in fluid communication with the inlet opening, wherein said device is at least partially composed of or comprises material which comprises materia! transformed into an optically modulating state, e.g. plastic material transformed into an optically modulating state.
  • material transformed into an optically modulating state refers to material as described herein above, e.g. material comprising a laser mark or marking or a marked surface wherein said mark or marking or marked surface is optically modulating or material obtained or obtainable with a method of transformation as defined herein above.
  • a microfiuidic device comprises a first channel having an inlet opening, an outlet and a longitudinal section between said inlet and said outlet wherein said device is at least partially composed of or comprises material which comprises material transformed into an optically modulating state, e.g. plastic material transformed into an optically modulating state.
  • material transformed into an optically modulating state refers to material as described herein above, e.g. material comprising a laser mark or marking or a marked surface wherein said mark or marking or marked surface is optically modulating or material obtained or obtainable with a method of transformat ion as defined herein above.
  • Further forms of the microfiuidic device are also envisaged, e.g. a microfiuidic device wherein only an inlet port is present, i.e. a self-contained device.
  • a microfiuidic device comprises a first channel having an inlet opening, an outlet, and a longitudinal section between said inlet opening and said outlet, wherein said device is at least partially composed of or comprises material which comprises material transformed into an optically modulating state, e.g. plastic material transformed into an optically modulating state.
  • material transformed into an optically modulating state refers to material as described herein above, e.g. material comprising a laser mark or marking or a marked surface wherein said mark or marking or marked surface is optically modulating or material obtained or obtainable with a method of transformation as defined herein above.
  • Further forms of the microfluidic device are also envisaged, e.g. a microfluidic device wherein only an iniet port is present, i.e. a self-contained device.
  • a microfluidic device comprises a channel including a capillary inlet; and a detection region in fluid communication with the capillary inlet; wherein said device is at least partially composed of or comprises material which comprises material transformed into an optically modulating state, e.g. plastic material transformed into an optically modulating state as described herein.
  • the capillary inlet and/or the detection region, and/or the channel including the inlet or outlet may comprise, partially comprise, be composed or be partially composed of said material.
  • Further forms of the device are also envisaged, e.g. devices wherein only an inlet port is present, i.e. self-contained devices or cartridges.
  • a microfluidic device in another embodiment, comprises a channel including a capillary inlet; and a detection region in fluid communication with the capillary inlet; and a microfluidic flow path having an at least partially deformable wall and being in fluid communication with the detection region of the channel; wherein said device is at least partially composed of or comprises material which comprises material transformed into an optically modulating state, e.g. plastic material transformed into an optically modulating state as described herein.
  • the capillary inlet and/or the detection region, and/or the microfluidic flow path, and/or the channel including the inlet or outlet, and/or the deformable wall section may comprise, partially comprise, be composed or be partially composed of said material.
  • Further forms of the device are also envisaged, e.g. devices wherein only an inlet port is present, i.e. self-contained devices or cartridges. Examples of such devices and further details are described in International Patent Application
  • a device e.g. suitable or envisaged for qualitatively and/or quantitatively detecting molecular interactions between probe molecules and target molecule, may comprise a micro-array comprising probe molecules immobilized in array elements, said micro-array being disposed on a first surface of the device; and a reaction chamber formed between the first surface including the micro-array disposed thereon, and a second surface, wherein said device is at least partially composed of or comprises material, which comprises material transformed into an optically modulating state, e.g. plastic material transformed into an optically modulating state as described herein.
  • the first surface of the device, the reaction chamber formed between the first surface including the micro- array disposed thereon, and/or the second surface may comprise, partially comprise, be composed or be partially composed of said material.
  • Further forms or derivatives of the device are also envisaged, e.g. devices wherein the micro-array may be disposed on the second surface.
  • the distance between micro-array and the second surface of the device may be variable. Examples of such devices and further details are described in International Patent Application WO 2005/108604 (which is incorporated by reference in its entirety).
  • a cartridge may comprise a microfluidic channel including a capillary inlet and a detection region in fluid communication with the capillary inlet, wherein said cartridge is at least partially composed of or comprises material which comprises material transformed into an optically modulating state, e.g. plastic material transformed into an optically modulating state as described herein.
  • the microfluidic channel, and/or the detection region, and/or the capillary inlet may comprise, partially comprise, be composed or be partially composed of said material.
  • Further forms or derivatives of the cartridge are also envisaged, e.g. cartridges comprising an outlet.
  • a device may comprise a first and second substrates defining a channel therebetween, at least one of the substrates being flexible, the channel comprising an array of spaced-apart test zones, each test zone comprising a probe compound configured to participate in an assay for a target analyte, wherein said device is at least partially composed of or comprises material which comprises material transformed into an optically modulating state, e.g. plastic material transformed into an optically modulating state as described herein.
  • the channel between the first and second substrates of the device, the reaction chamber formed between the first surface including the micro-array and/or one or more test zones may comprise, partially comprise, be composed or be partially composed of said material. Further forms or derivatives of the device are also envisaged. Examples of such devices and further details are described in
  • a device in another aspect, comprises a reaction chamber f ormed within a chamber body between a first surface and a second surface, wherein said device is at least partially composed of or comprises material which comprises material transformed into an optically modulating state, e.g. plastic material transformed into an optically modulating state as described herein.
  • the first surface and/or second surface may comprise, partially comprise, be composed or be partially composed of said material. Further forms or derivatives of the device are also envisaged, e.g. devices wherein the first surface comprises a micro-array.
  • a device e.g. suitable or envisaged for qualitative and/or quantitative detection of particles, may comprise a reaction chamber formed within a chamber body between a first surface and a second surface, wherein the second surface is located opposite to the first surface, and a micro fluidic flow path having an at least partially deformable wall, being in fluid communication with the reaction chamber, wherein said device is at least partially composed of or comprises material which comprises material transformed into an optically modulating state, e.g. plastic material transformed into an optically modulating state as described herein.
  • the device may comprise one or more optically modulating elements located on either the first or the second surface of the reaction chamber.
  • the device may comprise one or more optically modulating elements on the first and the second surface and/or in the micro fluidic flow path.
  • the first surface and/or second surface may comprise, partially comprise, be composed or be partially composed of said material.
  • Further forms or derivatives of the device are also envisaged, e.g. devices wherein the first surface comprises a micro-array and/or wherein the distance between the micro-array and the second surface is variable.
  • devices comprising a micro-array on the first surface may further comprise one or more optically modulating elements on the first surface of the reaction chamber. The number of the modulating elements may vary in dependence of the size of the device, its purpose, the size and form of the elements or other factors.
  • between about 1 to 1 000, e.g. about 10, 20, 30, 40, 50, 60, 70, 80, 90, 100 or more than 100, e.g. about 150, 200, 250, 300, 350, 400, 450, 500, 550, 600, 650, 700, 750, 800, 850, 900, 950, or 1000, or any natural number in between these numbers, or more than 1 OOOoptically modulating elements may be located.
  • a device e.g. suitable or envisaged for qualitative and/or quantitative detection of particles, e.g. cells, including, for example, T-helper cells or CD4 + T-cells, may comprise a reaction chamber formed within a chamber body between a first surface and a second surface, wherein the second surface is located opposite to the first surface; and one or more displacers, wherein the distance between the first surface and the second surface is variable via the one or more displacers at least in one or more parts of the surface area of the first surface and/or the second surface, wherein said device is at least partially composed of or comprises material which comprises material transformed into an optically modulating state, e.g. plastic material transformed into an optically modulating state as described herein.
  • an optically modulating state e.g. plastic material transformed into an optically modulating state as described herein.
  • first surface and/or second surface and/or the displacer may comprise, partially comprise, be composed or be partially composed of said material.
  • Further forms or derivatives of the device are also envisaged, e.g. devices wherein the first surface comprises a micro-array and/or wherein the distance between the micro-array and the second surface is variable and wherein the second surface has a displacement structure and/or wherein the displacer or displacement structure is not part of the device, but provided by an external entity. Examples of such devices and further details are described in International Patent Application WO 2007/051863.
  • a device e.g. suitable or envisaged for detecting an analyte, may comprise a cartridge having a microfluidic channel including a capillary inlet; and a detection region in fluid communication with the capillary inlet; a microfluidic flow path having an at least partially deformable wall and in fluid communication with the detection region of the channel; and a control element, e.g. as defined herein above, wherein said device is at least partially composed of or comprises material which comprises material transformed into an optically modulating state, e.g. plastic material transformed into an optically modulating state as described herein.
  • the microfluidic channel, and/or the capillary inlet, and/or the detection region, and/or the microfluidic path, and/or the partially deformable wall and/or the control element may comprise, partially comprise, be composed of or be partially composed of said material.
  • Further forms or derivatives of the device are also envisaged, e.g. devices additionally comprising a cap comprising a sealing member configured to seal with the inlet and form a fluid circuit including the inlet, the microfluidic channel and the microfluidic flow path. Examples of such devices and further details are described in International Patent Application WO 2008/135564.
  • a device e.g. suitable or envisaged for detecting an analyte, may comprise a cartridge having a microfluidic channel including a capillary inlet; and a detection region in fluid communication with the capillary inlet; a microfluidic flow path having an at least partially deformable wall and in fluid communication with the detection region of the channel; and a cap comprising a sealing member configured to seal with the inlet and form a fluid circuit including the inlet, the microfluidic channel and the microfluidic flow path, wherein said device i at least partially composed of or comprises material which comprises material transformed into an optically modulating state, e.g. plastic material transformed into an optically modulating state as described herein.
  • an optically modulating state e.g. plastic material transformed into an optically modulating state as described herein.
  • the microfluidic channel, and/or the capillary inlet, and/or the detection region, and/or the microfluidic path, and/or the partially deformable wall may comprise, partially comprise, be composed of or be partially composed of said material. Examples of such devices and further details are described in International Patent Application WO 2008/135564.
  • a system e.g. suitable or envisaged for detecting an analytc, comprises a cartridge having a microfluidic channel including an inlet and a detection region in fluid communication with the inlet; a microfluidic flow path having an at least partially deformable wall and in fluid communication with the detection region of the channel; and a cap comprising a sealing member configured to seal with the inlet and form a fluid circuit including the inlet, the microfluidic channel and the microfluidic flow path; and an optical or fluorescence detector including a light source; a condenser lens; and an objective lens; wherein said system is at least partially composed of or comprises material which comprises material transformed into an optically modulating state, e.g.
  • the condenser Jens may be a condenser lens obtaining a solid angle of 10° or greater.
  • the objective lens may be an objective lens obtaining a solid angle of 10° or greater.
  • the microfluidic channel, and/or the inlet, and/or the detection region, and/or the microfluidic path may comprise, partially comprise, be composed of or be partially composed of said material. Further forms or derivatives of the system are also envisaged, e.g. devices which have no optical or fluorescence detector, devices which have a detector for non-fluorescent light, systems without a cap structure. Examples of such systems and further details are described in International Patent Application WO 2010/105802 (which is incorporated by reference in its entirety).
  • a device or system is a device, system or derivative thereof as described, for example, in International Patent Application
  • WO 2008/055915 or WO 2009/013321 wherein said device or system is at least partially composed of or comprises material which comprises material transformed into an optically modulating state, e.g. plastic material transformed into an optically modulating state as described herein.
  • a device e.g.
  • suitable or envisaged for detecting an analyte in a sample comprises a cartridge having a microfluidic channel including a capillary inlet; and a detection region in fluid communication with the capillary inlet; a microfluidic flow path having an at least partial iy deformable wall and in fluid communication with the detection region of the channel; and a control element, wherein said control element is at least partially composed of or comprises material which comprises material transformed into an optically modulating state, e.g. plastic material transformed into an optically modulating state as described herein.
  • the control element may be a control element as described herein.
  • said control element may be associated with the control of an optical parameter as described herein.
  • said control element may be employed in a method of determining the focus as described herein above.
  • a device, a system or a cartridge as described herein comprise one or more optically modulating elements.
  • Such elements may, for example, comprise geometrical forms, geometrical pattern, spots, dots, lines, circles, squares, characters, symbols, drawings, barcodes, datamatrixcodes or datamatrixes, or any combination thereof.
  • said geometrical forms are those described herein above.
  • a device, a system or a cartridge as described herein comprise an array of optically modulating spots.
  • Such elements may, for example be present as a geometrically ordered array, or be present in the form of a barcode, character or in any other form or shape.
  • the array may, for example, comprise 2 spots, 3, 4, 5, 6, 7, 8, 9, 10, 20, 30, 40, 50, 60, 70, 80, 90, 100, 200, 300, 500, 1000 or more than thousand spots per unit or surface of the device, system or cartridge.
  • said array of optically modulating spots may be in the form of a datamatrix or reference mark, e.g. as described herein above.
  • said a device, a system or a cartridge as described herein is at least partially composed of or comprises material as defined herein above, e.g. plastic material, or combinations of plastic material with other material as defined herein above.
  • a method e.g. suitable or envisaged for the qualitative and/or quantitative detection of particles, e.g. cells, including, for example, T-helper cells or CD4 + T-cells as mentioned herein above or below, may comprise positioning a sample supposed to comprise one or more species of particles to be detected in a reaction chamber comprised in a device as described herein, e.g. a device at least partially composed of or comprising material which comprises material transformed into an optically modulating state, e.g.
  • the method may additionally comprise an optical control step as described herein above, e.g. the controlling of the checking or adjusting of the focus if necessary.
  • the method may comprise positioning a sample comprising multiple particles in a reaction chamber, displacing a subset of said multiple particles within the reaction chamber via the one or more displacers, determining one or more values indicative for the number of the subset of particles displaced within the reaction chamber, and optionally calculating the total number of the multiple particles in the reaction chamber from the one or more values obtained during detection.
  • the method further comprises
  • the one or more agents may be selected from the group consisting of nucleic acids, peptides, protein domains, proteins, carbohydrates, low molecular weight chemical compounds, and analogs and/or mixtures thereof and have binding affinity for one or more particles to be detected.
  • method may comprise positioning multiple particles of a sample within a detection chamber, displacing some of the multiple particles from the detection chamber so that only a proper subset of the multiple particles remains, optically detecting particles of the subset of multiple particles, and based on the detected particles, determining a value indicative of the number of particles of the subset of particles.
  • the method further comprises determining a value indicative of a number or abundance of particles in the sample based on the value indicative of the number of particles of the proper subset. Optionally, this determination is further based on a size of a detection volume of the detection chamber. In an additional embodiments, the method further comprises repeating a number NR. times the steps of positioning multiple particles of the sample within the detection chamber and displacing some of the multiple particles from the detection chamber so that, in each case, only a proper subset of the multiple particles remains, and where NR > 2 and, for a number ND of the NR.
  • the method comprises repeating NR times the steps of positioning and displacing comprises, for multiple of the NR repetitions, reintroducing at least some of the displaced multiple particles to the detection chamber.
  • displacing some of the multiple particles may comprise reducing a volume of the detection chamber which, in turn, may comprise reducing a distance between first and second walls of the chamber.
  • the method may comprise positioning multiple particles of a sample within a detection chamber, displacing some of the multiple particles from the detection chamber so that only a proper subset of the multiple particles remains, optically detecting particles of the subset of multiple particles, and determining the presence of a target particle among the subset of particles.
  • the method comprises positioning a first multiple of particles of a sample within a detection chamber, reducing a volume of the detection chamber, optically detecting particles within the detection chamber, based on the detected particles, determining a value indicative of the number of particles present within the detection chamber, increasing a volume of the detection chamber, positioning a second multiple of particles of the sample within the detection chamber, reducing a volume of the detection chamber, and based on the detected particles, determining a value indicative of the number of particles present within the detection chamber. Examples of such methods and further details are described in International Patent Application WO 2007/051861 (which is incorporated by reference in its entirety).
  • a method may comprise labeling particles, e.g. cells, including, for example, T-he!per cells or CD4 + T-cells as mentioned herein below, immobilized in the microfiuidic channel of a device or system with an optical label or labeling reagent; obtaining a first image comprising at least a subset of the immobilized particles; determining a first value indicative for the number of particles in the first image; obtaining a further image of the subset of immobilized particles after an interim; determining a further value indicative for the number of particles in the further image; determining a third value indicative for the activity and/or quality of the optical label or labeling reagent and/or the quality of an interaction between a particle and a labeling reagent and/or the usability of the device or system and/or of any procedure, function or method carried out with or in said device or system and/or the accuracy of a test result obtained by using said device or system, based on a comparison of the first value and the further value
  • the step of obtaining a further image and determining a further value can be repeated at least 2, 3, 5, 10 or n times and the determination of the third value can be based on a comparison of the first and the further value(s).
  • the third value indicative for the quality o the labeling reagent and/or the quality of an interaction between a particle and a labeling reagent and/or the usability of the device or system and/or of any procedure, function or method carried out with or in said device or system can be an increase of the further value with respect to the first value by at least about 10%, at least about 20% or by at least about 30%.
  • the third value may be compared with a threshold value. Based on this comparison, an action may result. In some embodiments, this action may be one or more of a group comprising displaying an error message, displaying a status message, moving a component relative to another component, performing an algorithm, aborting or continuing an assay, procedure, algorithm etc.
  • an increase of the further value with respect to the first value or a threshold value of more than about less than about 10%, less than about 20% or less than about 30% can indicate the non-usability of the device or system and/or of any procedure or method carried out with or in said device or system. Obtaining such an increase can lead to a discontinuation of usage of said device or system and/or a disregard of results obtained with said device or system.
  • a particle immobilized in the micro fluidic channel may be an inorganic substance, a eukaryotic cell, e.g. a mammalian cell, including, for example, a T-helper cell or CD4 + T-cell as mentioned herein below, a bacterium, or a virus.
  • the labeling reagent to be used in the method may be a dye, a ligand or an antibody.
  • the dye, ligand or antibody can be fluorescent or conjugated to a fluorescent element.
  • the interim between a first and a further image can be between about 10 sec and 30 min, between about 1 min and 15 min, between about 5 min and 10 min, or about 7 min.
  • the method comprises: obtaining an image of at least one position of a micro fluidic channel comprised in a device or system; introducing a sample into the microfluidic channel; obtaining a further image of the at least one position of a microfluidic channel; analyzing one or more parameters of the images; calculating a value indicative for the presence of a sample in the microfluidic channel and/or the usability of the device or system and/or of any procedure, function or method carried out with or in said device or system, based on the analyzed parameters.
  • the parameter of the image to be used can be a grey value in each image.
  • the value indicative for the presence of a sample in the microfluidic channel and/or the usability of the device or system and/or of any procedure, function or method carried out with or in said device or system can be an increase of the grey value by more than about 50% between the grey value in said image and the grey value in said further image. Obtaining such a value can lead to a continuation of usage of said device or system and/or a confirmation of results obtained with said device or system.
  • an increase of said grey values by less than about 50% between said image and said further image can indicate the non- presence of a sample in the microfluidie channel and/or the non-usability of the device or system and/or of any procedure or method carried out with or in said device or system.
  • the parameter of the image to be used is the 50 th to 95 th percentile or the 90 th percentile of the grey values in each image.
  • the method may additionally comprises: checking the focus of a detection unit of a system or associated with a device, wherein said system or device comprises one or more optically detectable particles being immobilized within a microfluidie channel, and adjusting the focus if necessary; adjusting the exposure time for the detection unit; optically detecting the one or more particles in a predefined area of the microfluidie channel; determining a first value indicative for the number of particles in said area; and determining a second value indicative for the usability of the device or system and/or of any procedure, function or method carried out with or in said device or system, based on a comparison of the first value with a threshold value; or the method, comprising: placing a lens at a first distance and at a first position with respect to a microfluidie channel o a device or system comprising a liquid sample and one or more optically detectable particles immobilized within a microfluidie channel, taking a first image of at least a subset of said immobilized particles, analyzing at
  • microfluidic channel of a device or system with an optical label or labeling reagent obtaining a first image comprising at least a subset of the immobilized particles; determining a first value indicative for the number of particles in the first image; obtaining a further image of the subset of immobilized particles after an interim; determining a further value indicative for the number of particles in the further image; determining a third value indicative for the activity and/or quality of the optical label or labeling reagent and/or the quality of an interaction between a particle and a labeling reagent and/or the usability of the device or system and/or of any procedure, function or method carried out with or in said device or system, based on a comparison of the first value and the further value, can be performed in combination with a method comprising: obtaining an image of at least one position of a microfluidic channel comprised in a device or system; introducing a sample into the microfluidic channel; obtaining a further image of the at least one position of a microflui
  • the method can further comprise at least one of the following steps: controlling the presence of a device within or with respect to a detection unit of a system; determining an optical, e.g. fluorescence background in the microfluidic channel of the device or system; determining a target counting plausibility via the detection of certain target particles in the device or system; controlling the moveability of the device within the detection unit of the system; controlling of accu charge, date plausibility and/or temperature in the device or system; and controlling of software parameters of the system.
  • the method comprises: introducing a liquid sample into a microfluidic channel disposed within a microfluidic network, device or system, wherein the microfluidic channel comprises the liquid sample comprising multiple particles, and wherein said microfluidic channel comprises and/or is associated with a control element; forming a mixture comprising at least a portion of the liquid sample and an optical label; forming multiple complexes, each complex comprising one of the multiple particles and at least one of the optical labels; detecting complexes present within a subset of the mixture; performing a control procedure comprising determining a value based on the control element and comparing the value with a predefined value; wherein a matching of both values or a deviation between both values of less than about 30% indicates the usability of the microfluidic channel, device or system and/or of any procedure, function or method carried out with or in said microfluidic channel, de vice or system, leading to a continuation of usage of said miro fluidic channel, device or system and/or a confirmation of
  • any of the methods may comprise a step of detecting complexes allowing a detection and/or a diagnosis of a retroviral infection and/or a conclusion on the status of a retroviral infection.
  • the retroviral infection may be an infection with HIV.
  • the method comprises: contacting particles immobilized within a microfluidic channel of a microfluidic network, device or system, e.g.
  • control element may be a control element as described herein. In one embodiment, the control element may be a control element as described herein. In one embodiment, the control element may be a control element as described herein. In one embodiment, the control element may be a control element as described herein. In one embodiment, the control element may be a control element as described herein. In one embodiment, the control element may be a control element as described herein. In one embodiment, the control element may be a control element as described herein. In one
  • control element may be associated with the control of an optical parameter as described herein.
  • said control element may be em loyed in a method of determining the focus as described herein above.
  • a method may comprise providing a device or system comprising material, e.g. plastic material, transformed into an optically modulating state wherein said material comprises a predetermined number of optically modulating elements and/or comprises optically modulating elements of a predetermined size; obtaining an image comprising at least a subset of the elements; determining the number and/or size of the elements comprised in said image;
  • material e.g. plastic material
  • the excitable element may be any optically modulating element as described above, e.g. a geometrical form, a geometrical pattern, a spot, dot, line, circle, square, character, symbol, drawing, barcode or datamatrix or datamatrixcode, or any combination thereof.
  • predetermined number refers to a fixed number of such elements, which may be obtained during the modification of a material, e.g. plastic material, as described herein.
  • the number of elements may also be encoded in a datamatrix or barcode being present in or on said device and/or being detectable with the same reader suitable for the determination of the number or size.
  • predetermined size refers to a fixed size of one or more such elements, which may be obtained during the modification of a material, e.g. plastic material, as described herein. Also the size of the elements may be encoded in a datamatrix or barcode being present in or on said device and/or being detectable with the same reader suitable for the determination of the number or size.
  • a detection unit may be comprised in a system, e.g. a system for performing assays such as biological, medical, chemical, biochemical assays, cell counting etc. or may be associated with a device wherein assays may be performed such as biological medical, chemical, biochemical assays, cell counting etc.
  • a comparison of the determined number and/or size and/or shape of the optically modulating elements, with said predetermined number and/or size leads to a difference
  • the focus of the reading device may be adjusted and/or the distance between the reading device and the material comprising the optically modulating elements may be modified or adjusted. This may be done automatically, e.g. with the help of electronic or mechanical devices, typically in the form of autofocussing on an object. Suitable techniques, devices, or calculation methods etc. are known to the person skilled in the art. Alternatively, theses parameters may be adjusted manually.
  • the exposure time for the detection unit may be ad justed according to the amount and intensity of light reaching the detection unit, e.g. in reaction to the depth of image field, the distance range over which objects are acceptably sharp or in focus or any other suitable parameter known to the person skilled in the art.
  • the adjustment may be carried out automatically, e.g. with the help of electronic or mechanical devices, typically in the form of an automated comparison to a lookup table. Suitable techniques, devices, lookup tables for threshold values etc. are known to the person skilled in the art.
  • the exposure time may be adjusted manually.
  • the chromatic aberration o a detection lens may be determined based on a comparison of the determined number and/or size and/or shape of the optically modulating elements, with said predetermined number and/or size, i , in a further specific embodiment, a comparison of the determined number and/or size of the optically modulating elements, with said predetermined number and/or size leads to a difference, the chromatic aberration of the detection lens may be adjusted.
  • light emission may be determined. For instance the light emission of the optically modulating elements present in the device or system may be determined. A correspondingly obtained value may be compared to a previously obtained and registered value for the light emission. If, in a further specific embodiment, a comparison of the determined light emission of the optically modulating elements, with said predetermined light emission leads to a difference, the focus, the exposure time and/or the chromatic aberration of the detection lens may be adjusted, e.g. as described herein.
  • difference refers to a deviation of more than about 1%, more than about or equal to 2%, more than about or equal to 3%, or more than about or equal to 4%, or more than about or equal to 5%, 6%, 7%, 8%, 9%, 10%, 1 1 %, 12%, 13%, 14%, 15%, 20%, 25%, or 30% deviation between the number and/or size of the optically modulating elements, with said predetermined number and/or size of said elements.
  • the device or system and/or any procedure, function or method carried out with or in said device or system may be considered as non-usablc.
  • the device or system and/or any procedure, function or method carried out with or in said device system may also be considered as non-usable. Otherwise, i.e. if the value is within a range, e.g.
  • the device or system and/or any procedure, function or method carried out with or in said device system may also be considered as usable and/or be confirmed. If a non-usability situation is encountered in this context the usage of the device or system may be discontinued and/or any results obtained may be disregarded.
  • Corresponding information may be recorded electronically or encoded in a barcode or datamatrix or any other suitable coding material. Such a barcode or datamatrix may, for instance, be attached to a device or microfluidic channel.
  • the method may additionally comprise positioning a sample supposed to comprise one or more species of particles to be detected in a reaction chamber comprised in the device; and detecting/determining a value indicative for the presence and/or number of one or more species of particles.
  • this additional step may be carried out once the usability of the device or system has been shown or confirmed. The detection may be carried out as described herein above.
  • the method may comprise displacing at least a part of the sample within the reaction chamber.
  • a displacement may be carried out with one or more displacers or displacer structures.
  • the material comprised in a device, a system or a cartridge as used in a method as described above may comprise an array of optically modulating spots.
  • Such elements may, for example be present as a geometrically ordered array, or be present in the form of a barcode, character or in any other form or shape.
  • the array may, for example, comprise 2 spots, 3, 4, 5, 6, 7, 8, 9, 10, 20, 30, 40, 50, 60, 70, 80, 90, 100, 200, 300, 500, 1000 or more than thousand spots per unit or surface of the device, system or cartridge.
  • the material comprised in a device, a system or a cartridge as used in a method as described above is at least partially composed of or comprises material as defined herein above, e.g. plastic material, or combinations of plastic material with other material as defined herein above.
  • the sample to be analysed as mentioned is a blood sample.
  • the blood sample is a sample of human blood.
  • the particle to be detected as mentioned herein, or to be measured or identified in a method as described above is a prokaryotic cell, eukaryotic cell, or a viral particle.
  • the particle is a human cell.
  • the particle is a T helper cell, e.g. a human T helper ceil.
  • the particle is a CD4 + T-celi, e.g. a human CD4* T-cell.
  • a cartridge which is partially composed of or comprises material as defined herein above is provided, wherein the cartridge (FIG. 7, Ref. 100) is suitable for the analysis of the number of cells, e.g. the number of T helper cells or of CD4 + T-cclls.
  • the cells may be derived from suitable samples, e.g. from a blood sample, in particular a clinical human blood sample.
  • the cartridge may comprise a detection channel (FIG. 7, Ref. 1 10).
  • the detection channel may comprise control elements for adjusting e.g. the focus position or the exposure time of a detector arranged relative to the detection channel, e.g. in a section of the detection channel (FIG. 7, Ref. 130).
  • the detection channel may comprise control elements for adjusting e.g. the focus position or the exposure time of a detector arranged relative to the detection channel and/or for checking of the chromatic aberration of a detection lens, e.g. in a section of the detection channel (FIG. 7, Ref. 130).
  • the cartridge may further comprise a capillary inlet suitable for the intake of a sample, e.g. a blood sample.
  • a sample e.g. a blood sample.
  • the cartridge may as well comprise a control for said capillary inlet (FIG. 7, Ref. 120).
  • the cartridge may comprise a predetermined range of one or more optically modulating singular spots (FIG. 7, Ref. 140).
  • the optically modulating spots may, in a further embodiment, have a defined geometric shape and specific optically modifying characteristics.
  • the optically modulating spots may be located on each individual cartridge at a defined position in the detection channel, e.g. in a section of the detection channel as depicted in FIG. 7, Ref. 130.
  • the method of transformation of material as described above may be used for the modification or generation of a microfluidic cartridge (FIG. 7, Ref. 100).
  • a cartridge comprising a detection channel (FIG. 7, Ref. 1 10), a capillary inlet, a control for a capillary inlet (FIG. 7, Ref. 120), and a predetermined range of one or more optically modulating singular spots having a defined geometric shape and specific optically modifying characteristics (FIG. 7, Ref. 140) located in the detection channel, or a cartridge as defined herein above, may be used for determining a number of cells in a blood sample.
  • the cells to be determined may be any cells.
  • the cells are T helper cells or CD4 + T- cells.
  • the determination of the number of cells may include a step of adjusting the focus position or the exposure time of a detector arranged relative to the detection channel, e.g. via control elements.
  • the determination of the number of cells may include a step of adjusting the focus position or the exposure time of a detector arranged relative to the detection channel via control elements such as one or more singular optically modulating spots having a defined geometric shape and specific optically modifying characteristics (FIG. 7, Ref. 140).
  • the determination of the number of cells may include a step of adjusting the focus and exposure time of the detection system and furthermore a check of the chromatic aberration of a detection lens, e.g. via control elements.
  • the determination of the number of cells may include a step of adjusting the focus and exposure time of the detection system and furthermore a check of the chromatic aberration of a detection lens via control elements such as one or more singular optically modulating spots having a defined geometric shape and specific optically modifying characteristics (FIG. 7, Ref. 140).
  • a correspondingly performed test or assay may be considered invalid and/or no test result but an error code may be displayed if a predefined threshold parameter is not reached.
  • a predefined threshold parameter is not reached.
  • the focus position or the exposure time of a detector arranged relative to the detection channel controlled via the one or more singular optically modulating spots having a defined geometric shape and specific optically modifying characteristics does not reach the predefined threshold.
  • Example 1 Preparation of colored dots by a laser with 1064 nm in
  • FIG. 2 A - B and 3A - B show a regular pattern of structures in a optically modulating state on a plastic surface.
  • a polystyrene plastic part containing 4% carbon black was beneath a 1064 nm laser.
  • the focus plain was adjusted by a standard method measuring the highest impact of the laser beam onto a surface.
  • the energy of the pulse can be influenced by the power of the diodes, which are needed to pulse the laser.
  • the frequency of the laser also influences the energy.
  • a laser pulse having a higher frequency results in a decrease of the energy of the laser beam.
  • FIG. 2 A and 3A show the surface as seen in a standard microscope (Zeiss Axioskop, l Ox magnification), FIG. 2B and 3B as seen in a fluorescence reader (excitation wavelength 520 nm).
  • a Nd : YAG laser with a maximum power of 8 W and a wavelength: of 1064 nm was used.
  • the frequency of the pulse was adjusted to 35 kHz at a pulse length of 5 ⁇ .
  • the power of the laser diodes was adjusted to 33% of the maximum power
  • the power of the laser diodes was adjusted to 29% of the maximum power.
  • Example 2 Determination of the morphology of transformed material with MEM microscopy
  • FIG. 4 A-E show REM pictures of the modificat ions created on the surface by using different laser energies. It could be shown that the spots' morphology is dependent on the energy applied. At a lower energy, spots appear to have more a spherical structure (see FIG. 4B and 4C). Higher energy leads to a burst of the spherical structures, as can be seen from FIG. 4D and 4E). All modifications were detected by using a fluorescence microscope.
  • the correlation between the signal intensity and the power of the laser was tested by creating optically modulating spots on a PS surface as described in example using a laser at different adjusted to different energies.
  • the surface was placed in a PIMA reader and the exposure time necessary for generating the same signal strength was measured.
  • the results of this experiment are depicted in the diagram of FIG 5 showing the relationship between the exposure time [ms] and the laser strength [A].
  • the exposure time may be shortened.
  • a higher laser power results in an increased amount of emitted light.
  • Example 4 Data Matrix Code written by the laser 355 nm on the PS surface It could further be shown that it is possible to use laser radiation in order to write datamatrix code on a PS surface.
  • the laser used was a 355 nm laser with 19.6 A and a frequency of 15 kHz. The results of this approach are depicted in FIG. 6.
  • the grid of the dots of the DMC is 50 ⁇ .
  • Example 5 Microfluidic cartridge comprising channel with structures in an optically modulating state
  • FIG. 8 shows a shifted regular pattern of structures in an optically modulating state on the surface of a channel of a microfluidic device as depicted in Fig. 7.
  • the body of the device made from polystyrene plastic part containing 4% carbon black was treated with a 355 nm Nd : YAG laser.
  • the focus plain of the laser was adjusted by a standard method measuring the highest impact of the laser beam onto a surface.
  • the energy of the pulse can be influenced by the power of the diodes, which are needed to pulse the laser.
  • the frequency of the laser also influences the energy.
  • a laser pulse having a higher frequency usually results in a decrease of the energy of the laser beam.
  • a Nd : YAG laser with a power of 2.1 W and a wavelength of 355 nm was used.
  • the frequency of the pulse was adjusted to 1 kHz at a pulse length of 1 .5 [is. Further the power of the laser beam was reduced by an optical instrument by 90%.
  • FIG. 8 A and B show the surface of the channel comprising the structures in an optically modulating state imaged by a PIMA Analyzer (Device serial number D- 000366, Alere Technologies GmbH).
  • the PIMA Analyzer includes fluorescent microscope functionality and has the capability to detect fluorescent signals at defined wavelengths, e.g. 593 nm and 685 nm while the excitation light is removed from detection by using filter elements.
  • the system software allows varying the exposure time and master gain within a certain range.
  • the master gain factor is multiplying the signal taken with camera with a defined factor.
  • FIG. 8A and 8B - show the structures in a optically modulating state excited at a standard excitation wavelength of the PIMA system at 520 nrtt. Itt Fig.
  • the image was detected at a wavelength of 593nm and an exposure time of 300ms and a master gain of 2.74, while tlie image shown in fig. SB was detected at 685nm with a ex.posu.re time of 300 ms and a master gain factor of 11.68.
  • the structures in an optically modulating state on the surface of the channel of tlie microfluidic device can be detected at a wavelength different to the excitation wavelength.
  • the structure can be used to adjust and /or control e.g. the focus position and/or the exposure time of the detection system of the PIMA system. And/or, as described herein, the structures can be used to serve as an internal control for assessing the. validity of the experiment results.
PCT/EP2011/071618 2010-12-03 2011-12-02 Transformation of material into an optically modulating state via laser radiation WO2012072795A2 (en)

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EP11802005.6A EP2646155A2 (de) 2010-12-03 2011-12-02 Transformation von materials in einen optisch modulierenden zustand über laserstrahlung
CN201180057678.8A CN103442809B (zh) 2010-12-03 2011-12-02 通过激光照射把材料转换成光学调制状态

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Families Citing this family (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP7406374B2 (ja) 2017-06-28 2023-12-27 ホヤ レンズ タイランド リミテッド 眼鏡レンズの製造方法、眼鏡レンズの製造システム、眼鏡レンズ
CN107286375A (zh) * 2017-07-26 2017-10-24 深圳市集美新材料股份有限公司 眼镜胶板及其制造方法
JP6484780B1 (ja) * 2018-04-03 2019-03-20 フォトメディカル合同会社 微弱光検出システムおよび微弱光検出方法
RU194514U1 (ru) * 2019-09-17 2019-12-13 Андрей Львович Степанов Счетная сетка в объеме стеклянной подложки для анализа биологических микрообъектов
RU2717684C1 (ru) * 2019-09-17 2020-03-25 Андрей Львович Степанов Счетная сетка в объеме стеклянной подложки для анализа биологических микрообъектов
WO2021117899A1 (en) * 2019-12-13 2021-06-17 Ricoh Company, Ltd. Substrate, container, product, production method, and production apparatus
CN111138703B (zh) * 2019-12-30 2022-02-15 四川大学 一种通过激光辐照聚合物树脂制备线型多烯类颜料的方法
CN112289172B (zh) * 2020-09-30 2022-08-16 北京德弦科技有限公司 宝石的数据标识加工方法

Citations (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4822973A (en) 1984-03-30 1989-04-18 Bayer Aktiengesellschaft Composite plastic with laser altered internal material properties
US6284184B1 (en) 1999-08-27 2001-09-04 Avaya Technology Corp Method of laser marking one or more colors on plastic substrates
WO2005108604A2 (de) 2004-05-06 2005-11-17 Clondiag Chip Technologies Gmbh Vorrichtung und verfahren zum nachweis von molekularen wechselwirkungen
WO2007051863A2 (en) 2005-11-04 2007-05-10 Clondiag Gmbh Method and device for the detection of molecular interactions
WO2007051861A1 (en) 2005-11-04 2007-05-10 Clondiag Gmbh Device and method for the detection of particles
WO2008055915A2 (en) 2006-11-06 2008-05-15 Clondiag Gmbh Device and process for assays using binding members
WO2008062048A2 (en) 2006-11-22 2008-05-29 Clondiag Gmbh Methods for optically detecting multiple analytes in a liquid sample with a compressible microfluidic device
WO2008135564A2 (en) 2007-05-03 2008-11-13 Clondiag Gmbh Assays
WO2009013321A2 (en) 2007-07-23 2009-01-29 Clondiag Gmbh Assays
WO2009112594A2 (en) 2008-03-14 2009-09-17 Clondiag Gmbh Assays
WO2010105802A2 (en) 2009-03-16 2010-09-23 Clondiag Gmbh Assays

Family Cites Families (25)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1989009989A1 (en) * 1988-04-12 1989-10-19 Dia Nippon Insatsu Kabushiki Kaisha Optical recording medium and method of manufacturing same
US5537144A (en) * 1990-06-11 1996-07-16 Revfo, Inc. Electro-optical display system for visually displaying polarized spatially multiplexed images of 3-D objects for use in stereoscopically viewing the same with high image quality and resolution
JPH0568196A (ja) * 1991-09-06 1993-03-19 Seiko Instr Inc ジヨイント変換相関器型測距・自動焦点装置およびその駆動方式
US5658413A (en) * 1994-10-19 1997-08-19 Hewlett-Packard Company Miniaturized planar columns in novel support media for liquid phase analysis
US5977514A (en) * 1997-06-13 1999-11-02 M.A. Hannacolor Controlled color laser marking of plastics
US6929030B2 (en) * 1999-06-28 2005-08-16 California Institute Of Technology Microfabricated elastomeric valve and pump systems
JP3780758B2 (ja) * 1999-07-21 2006-05-31 セイコーエプソン株式会社 プラスチックレンズの製造方法
US6939587B1 (en) * 1999-09-03 2005-09-06 Kent State University Fabrication of aligned crystal cell/film by simultaneous alignment and phase separation
JP2001192036A (ja) * 1999-11-01 2001-07-17 Lion Corp 容器、および文字・図形の形成方法
AU2001261462A1 (en) * 2000-05-12 2001-11-26 University Of Cincinnati Structurally programmable microfluidic systems
JP3718131B2 (ja) * 2001-03-16 2005-11-16 松下電器産業株式会社 高周波モジュールおよびその製造方法
US7169471B1 (en) * 2003-02-06 2007-01-30 Emd Chemicals, Inc. Laser-marking additive
JP2004337958A (ja) * 2003-05-19 2004-12-02 Fuji Photo Film Co Ltd マーキング判定方法及びマーキング判定装置
US20050244984A1 (en) * 2004-04-28 2005-11-03 Parker Russell A Methods and compositions for calibrating chemical array readers
TW200616232A (en) * 2004-08-09 2006-05-16 Adv Lcd Tech Dev Ct Co Ltd Semiconductor device including semiconductor thin film, which is subjected to heat treatment to have alignment mark, crystallizing method for the semiconductor thin film, and crystallizing apparatus for the semiconductor thin film
CN101663576B (zh) * 2005-04-12 2012-05-23 卡钳生命科学股份有限公司 用于微流体器件的紧凑型光检测系统
FR2885071B1 (fr) 2005-04-28 2010-02-12 Becton Dickinson France Procede d'identification d'un contenant et/ou d'un article fini obtenu a partir dudit contenant, en particulier a usage medical
US8530785B2 (en) * 2005-08-02 2013-09-10 Merck Patent Gmbh Method for laser-marking and an article marked by such method
DE102005057474A1 (de) * 2005-11-30 2007-05-31 Merck Patent Gmbh Lasertransfer von Sicherheitsmerkmalen
ATE491582T1 (de) * 2006-11-07 2011-01-15 Basf Se Lasermarkierung von pigmentierten substraten
WO2009029513A1 (en) * 2007-08-24 2009-03-05 Armark Authentication Technologies, Llc Method for production of covert markers
CN101396883B (zh) * 2007-09-24 2012-10-17 3M创新有限公司 可用激光非接触式标记的标签、其制作方法及标记方法
JP5467670B2 (ja) * 2008-03-31 2014-04-09 株式会社ニデック 染色方法及び染色装置
CN101564947B (zh) * 2009-05-25 2010-12-08 深圳市大族激光科技股份有限公司 一种在塑料上的激光标记方法
JP5650390B2 (ja) * 2009-10-27 2015-01-07 日清ペットフード株式会社 ペットフード

Patent Citations (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4822973A (en) 1984-03-30 1989-04-18 Bayer Aktiengesellschaft Composite plastic with laser altered internal material properties
US6284184B1 (en) 1999-08-27 2001-09-04 Avaya Technology Corp Method of laser marking one or more colors on plastic substrates
WO2005108604A2 (de) 2004-05-06 2005-11-17 Clondiag Chip Technologies Gmbh Vorrichtung und verfahren zum nachweis von molekularen wechselwirkungen
WO2007051863A2 (en) 2005-11-04 2007-05-10 Clondiag Gmbh Method and device for the detection of molecular interactions
WO2007051861A1 (en) 2005-11-04 2007-05-10 Clondiag Gmbh Device and method for the detection of particles
WO2008055915A2 (en) 2006-11-06 2008-05-15 Clondiag Gmbh Device and process for assays using binding members
WO2008062048A2 (en) 2006-11-22 2008-05-29 Clondiag Gmbh Methods for optically detecting multiple analytes in a liquid sample with a compressible microfluidic device
WO2008135564A2 (en) 2007-05-03 2008-11-13 Clondiag Gmbh Assays
WO2009013321A2 (en) 2007-07-23 2009-01-29 Clondiag Gmbh Assays
WO2009112594A2 (en) 2008-03-14 2009-09-17 Clondiag Gmbh Assays
WO2010105802A2 (en) 2009-03-16 2010-09-23 Clondiag Gmbh Assays

Non-Patent Citations (3)

* Cited by examiner, † Cited by third party
Title
NAM-TRUNG NGUYEN; STEVE WERELEY: "Fundamentals and Applications of Microfluidics", 2002, ARTECH HOUSE PUBLISHERS
OLIVER GERIKE ET AL.: "Microsystem Engineering of Lab-on-a-Chip Devices", 2008, WILEY-VCH
See also references of EP2646155A2

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US9952153B2 (en) 2018-04-24
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